14-100758829-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758829
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758829
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 34266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*221G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.505G>C
  hgvsp: ENSP00000450913.1:p.Val169Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.505G>C
  hgvsp: ENSP00000442985.1:p.Val169Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1161C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.703G>C
  hgvsp: ENSP00000352167.3:p.Val235Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*667G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.505G>C
  hgvsp: ENSP00000452446.1:p.Val169Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.505G>C
  hgvsp: ENSP00000452078.1:p.Val169Leu
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7909
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31559
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10024
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9910
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val235Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-100758832-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758832
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758832
    reference: chr 14
allele count: 2
allele frequency: 5.690547999772378e-5
allele num: 35146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*664T>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.502T>G
  hgvsp: ENSP00000452446.1:p.Cys168Gly
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1164A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.502T>G
  hgvsp: ENSP00000450913.1:p.Cys168Gly
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.700T>G
  hgvsp: ENSP00000352167.3:p.Cys234Gly
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*218T>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.502T>G
  hgvsp: ENSP00000452078.1:p.Cys168Gly
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.502T>G
  hgvsp: ENSP00000442985.1:p.Cys168Gly
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31439
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys234Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

14-100758835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758835
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758835
    reference: chr 14
allele count: 2
allele frequency: 5.653870074065698e-5
allele num: 35374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.499G>A
  hgvsp: ENSP00000452078.1:p.Asp167Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.499G>A
  hgvsp: ENSP00000450913.1:p.Asp167Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.499G>A
  hgvsp: ENSP00000442985.1:p.Asp167Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*215G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1167C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.697G>A
  hgvsp: ENSP00000352167.3:p.Asp233Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*661G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.499G>A
  hgvsp: ENSP00000452446.1:p.Asp167Asn
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31195
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9837
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9800
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp233Asn
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

14-100758838-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758838
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758838
    reference: chr 14
allele count: 2
allele frequency: 5.658669081032141e-5
allele num: 35344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*212C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.496C>T
  hgvsp: ENST00000554912.1:c.496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.496C>T
  hgvsp: ENST00000556505.1:c.496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.496C>T
  hgvsp: ENST00000555927.1:c.496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.496C>T
  hgvsp: ENST00000539621.1:c.496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.694C>T
  hgvsp: ENST00000359232.3:c.694C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*658C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1170G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9835
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2058
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu232Leu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS

14-100758841-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758841
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758841
    reference: chr 14
allele count: 56
allele frequency: 1.563372417643774e-3
allele num: 35820
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.691A>G
  hgvsp: ENSP00000352167.3:p.Ile231Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.493A>G
  hgvsp: ENSP00000452078.1:p.Ile165Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.493A>G
  hgvsp: ENSP00000450913.1:p.Ile165Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*655A>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1173T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.493A>G
  hgvsp: ENSP00000452446.1:p.Ile165Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.493A>G
  hgvsp: ENSP00000442985.1:p.Ile165Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*209A>G
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 1.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30893
  bin: 7.5e0
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6155
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Ile231Val
num of homozygotes: 1
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

14-100758846-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758846
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758846
    reference: chr 14
allele count: 1
allele frequency: 2.75512453162883e-5
allele num: 36296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.488G>A
  hgvsp: ENSP00000450913.1:p.Arg163His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*650G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.488G>A
  hgvsp: ENSP00000442985.1:p.Arg163His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.488G>A
  hgvsp: ENSP00000452078.1:p.Arg163His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.488G>A
  hgvsp: ENSP00000452446.1:p.Arg163His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.686G>A
  hgvsp: ENSP00000352167.3:p.Arg229His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*204G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1178C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9615
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9653
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg229His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

14-100758852-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758852
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758852
    reference: chr 14
allele count: 3
allele frequency: 8.099352051835853e-5
allele num: 37040
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.680G>C
  hgvsp: ENSP00000352167.3:p.Arg227Pro
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.482G>C
  hgvsp: ENSP00000442985.1:p.Arg161Pro
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.482G>C
  hgvsp: ENSP00000452078.1:p.Arg161Pro
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*198G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.482G>C
  hgvsp: ENSP00000452446.1:p.Arg161Pro
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.482G>C
  hgvsp: ENSP00000450913.1:p.Arg161Pro
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*644G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1184C>G
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28695
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg227Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

14-100758853-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758853
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758853
    reference: chr 14
allele count: 1
allele frequency: 2.655901412939552e-5
allele num: 37652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.481C>T
  hgvsp: ENSP00000450913.1:p.Arg161Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.481C>T
  hgvsp: ENSP00000442985.1:p.Arg161Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*643C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1185G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.679C>T
  hgvsp: ENSP00000352167.3:p.Arg227Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.481C>T
  hgvsp: ENSP00000452078.1:p.Arg161Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*197C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.481C>T
  hgvsp: ENSP00000452446.1:p.Arg161Cys
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30633
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29620
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9245
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg227Cys
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

14-100758858-GCGCCCCGCAGTCCGTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758858
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758842
    reference: chr 14
allele count: 1
allele frequency: 2.575063089045682e-5
allele num: 38834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsp: ENSP00000442985.1:p.Asp154ProfsTer122
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsp: ENSP00000450913.1:p.Asp154ProfsTer122
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsp: ENSP00000352167.3:p.Asp220ProfsTer122
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsp: ENSP00000452446.1:p.Asp154ProfsTer122
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsp: ENSP00000452078.1:p.Asp154ProfsTer?
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2555
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp220ProfsTer122
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: GCGCCCCGCAGTCCGTC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

14-100758860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758860
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758860
    reference: chr 14
allele count: 2
allele frequency: 5.104905814487722e-5
allele num: 39178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.474C>T
  hgvsp: ENST00000554912.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*636C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.474C>T
  hgvsp: ENST00000556505.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*190C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.474C>T
  hgvsp: ENST00000539621.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.672C>T
  hgvsp: ENST00000359232.3:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.474C>T
  hgvsp: ENST00000555927.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1192G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8998
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30232
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6680
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8718
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly224Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-100758861-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758861
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758861
    reference: chr 14
allele count: 1
allele frequency: 2.516862981979261e-5
allele num: 39732
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1193C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.671G>A
  hgvsp: ENSP00000352167.3:p.Gly224Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*635G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.473G>A
  hgvsp: ENSP00000450913.1:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.473G>A
  hgvsp: ENSP00000452446.1:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.473G>A
  hgvsp: ENSP00000442985.1:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.473G>A
  hgvsp: ENSP00000452078.1:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*189G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8937
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29629
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2563
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly224Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

14-100758863-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758863
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758863
    reference: chr 14
allele count: 1
allele frequency: 2.488304966656714e-5
allele num: 40188
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.669G>A
  hgvsp: ENST00000359232.3:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.471G>A
  hgvsp: ENST00000554912.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.471G>A
  hgvsp: ENST00000539621.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.471G>A
  hgvsp: ENST00000555927.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*633G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*187G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1195C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.471G>A
  hgvsp: ENST00000556505.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*633G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8921
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1908
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29870
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg223Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

14-100758870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758870
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758870
    reference: chr 14
allele count: 1
allele frequency: 2.392344497607656e-5
allele num: 41800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*626G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.662G>A
  hgvsp: ENSP00000352167.3:p.Gly221Glu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.464G>A
  hgvsp: ENSP00000452446.1:p.Gly155Glu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.464G>A
  hgvsp: ENSP00000452078.1:p.Gly155Glu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1202C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.464G>A
  hgvsp: ENSP00000442985.1:p.Gly155Glu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*180G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.464G>A
  hgvsp: ENSP00000450913.1:p.Gly155Glu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*626G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30100
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7958
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly221Glu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

14-100758875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758875
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758875
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 44426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.459G>A
  hgvsp: ENST00000554912.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.459G>A
  hgvsp: ENST00000556505.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*175G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1207C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*621G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.657G>A
  hgvsp: ENST00000359232.3:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.459G>A
  hgvsp: ENST00000539621.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.459G>A
  hgvsp: ENST00000555927.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*621G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29696
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7186
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Ala219Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

14-100758876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758876
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758876
    reference: chr 14
allele count: 1
allele frequency: 2.220939013014703e-5
allele num: 45026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.458C>T
  hgvsp: ENSP00000450913.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.656C>T
  hgvsp: ENSP00000352167.3:p.Ala219Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.458C>T
  hgvsp: ENSP00000452446.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*620C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*620C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.458C>T
  hgvsp: ENSP00000442985.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*174C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.458C>T
  hgvsp: ENSP00000452078.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1208G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala219Val
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

14-100758877-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758877
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758877
    reference: chr 14
allele count: 1
allele frequency: 2.189237707430273e-5
allele num: 45678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*173G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.457G>A
  hgvsp: ENSP00000452078.1:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*619G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.457G>A
  hgvsp: ENSP00000450913.1:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.457G>A
  hgvsp: ENSP00000452446.1:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.655G>A
  hgvsp: ENSP00000352167.3:p.Ala219Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*619G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.457G>A
  hgvsp: ENSP00000442985.1:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1209C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31381
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala219Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

14-100758886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758886
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758886
    reference: chr 14
allele count: 1
allele frequency: 2.051197899573351e-5
allele num: 48752
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.646C>T
  hgvsp: ENSP00000352167.3:p.Arg216Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.448C>T
  hgvsp: ENSP00000442985.1:p.Arg150Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*610C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*610C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1218G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.448C>T
  hgvsp: ENSP00000452078.1:p.Arg150Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.448C>T
  hgvsp: ENSP00000452446.1:p.Arg150Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*164C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.448C>T
  hgvsp: ENSP00000450913.1:p.Arg150Trp
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29566
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5632
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg216Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

14-100758890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758890
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758890
    reference: chr 14
allele count: 3
allele frequency: 5.919027701049641e-5
allele num: 50684
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1222C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.444G>A
  hgvsp: ENST00000554912.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*160G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.642G>A
  hgvsp: ENST00000359232.3:c.642G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*606G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.444G>A
  hgvsp: ENST00000556505.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.444G>A
  hgvsp: ENST00000555927.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*606G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.444G>A
  hgvsp: ENST00000539621.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys214Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

14-100758899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758899
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758899
    reference: chr 14
allele count: 3
allele frequency: 5.617556737323047e-5
allele num: 53404
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.633C>T
  hgvsp: ENST00000359232.3:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1231G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*151C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.435C>T
  hgvsp: ENST00000554912.1:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*597C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.435C>T
  hgvsp: ENST00000539621.1:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.435C>T
  hgvsp: ENST00000555927.1:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.435C>T
  hgvsp: ENST00000556505.1:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*597C>T
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9860
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4638
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31256
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp211Asp
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

14-100758908-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758908
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758908
    reference: chr 14
allele count: 4
allele frequency: 7.121492664862555e-5
allele num: 56168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.426T>C
  hgvsp: ENST00000555927.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.624T>C
  hgvsp: ENST00000359232.3:c.624T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*588T>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*142T>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.426T>C
  hgvsp: ENST00000554912.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.426T>C
  hgvsp: ENST00000539621.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.426T>C
  hgvsp: ENST00000556505.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1240A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*588T>C
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27459
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11953
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2860
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr208Tyr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-100758910-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758910
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758910
    reference: chr 14
allele count: 2
allele frequency: 3.534068419564603e-5
allele num: 56592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*586T>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*586T>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.424T>C
  hgvsp: ENSP00000452078.1:p.Tyr142His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.424T>C
  hgvsp: ENSP00000442985.1:p.Tyr142His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.424T>C
  hgvsp: ENSP00000450913.1:p.Tyr142His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.424T>C
  hgvsp: ENSP00000452446.1:p.Tyr142His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*140T>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.622T>C
  hgvsp: ENSP00000352167.3:p.Tyr208His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1242A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10041
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30544
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr208His
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

14-100758911-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758911
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758911
    reference: chr 14
allele count: 2
allele frequency: 3.527834615113243e-5
allele num: 56692
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1243G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.423C>T
  hgvsp: ENST00000556505.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*585C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.423C>T
  hgvsp: ENST00000555927.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.423C>T
  hgvsp: ENST00000539621.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.423C>T
  hgvsp: ENST00000554912.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.621C>T
  hgvsp: ENST00000359232.3:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*139C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*585C>T
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr207Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

14-100758913-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758913
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758913
    reference: chr 14
allele count: 1
allele frequency: 1.753955168905883e-5
allele num: 57014
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.421A>G
  hgvsp: ENSP00000452078.1:p.Thr141Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*583A>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.421A>G
  hgvsp: ENSP00000450913.1:p.Thr141Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.421A>G
  hgvsp: ENSP00000452446.1:p.Thr141Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*583A>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.421A>G
  hgvsp: ENSP00000442985.1:p.Thr141Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1245T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*137A>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.619A>G
  hgvsp: ENSP00000352167.3:p.Thr207Ala
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2926
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr207Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

14-100758924-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758924
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758924
    reference: chr 14
allele count: 2
allele frequency: 3.365983372042142e-5
allele num: 59418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*572C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.410C>T
  hgvsp: ENSP00000452446.1:p.Ser137Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.608C>T
  hgvsp: ENSP00000352167.3:p.Ser203Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.410C>T
  hgvsp: ENSP00000442985.1:p.Ser137Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.410C>T
  hgvsp: ENSP00000450913.1:p.Ser137Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*126C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.410C>T
  hgvsp: ENSP00000452078.1:p.Ser137Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*572C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1256G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10763
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser203Phe
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: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

14-100758924-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758924
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758924
    reference: chr 14
allele count: 2
allele frequency: 3.365983372042142e-5
allele num: 59418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*572C>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*126C>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.410C>G
  hgvsp: ENSP00000452446.1:p.Ser137Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.410C>G
  hgvsp: ENSP00000452078.1:p.Ser137Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.410C>G
  hgvsp: ENSP00000442985.1:p.Ser137Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1256G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.410C>G
  hgvsp: ENSP00000450913.1:p.Ser137Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.608C>G
  hgvsp: ENSP00000352167.3:p.Ser203Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*572C>G
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10763
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3099
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser203Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD

14-100758928-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758928
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758928
    reference: chr 14
allele count: 2
allele frequency: 3.366776648037169e-5
allele num: 59404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*568G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.604G>A
  hgvsp: ENSP00000352167.3:p.Val202Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1260C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*122G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.406G>A
  hgvsp: ENSP00000450913.1:p.Val136Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.406G>A
  hgvsp: ENSP00000442985.1:p.Val136Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.406G>A
  hgvsp: ENSP00000452446.1:p.Val136Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.406G>A
  hgvsp: ENSP00000452078.1:p.Val136Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*568G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val202Met
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

14-100758948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758948
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758948
    reference: chr 14
allele count: 3
allele frequency: 4.549728532864206e-5
allele num: 65938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.386C>T
  hgvsp: ENSP00000452078.1:p.Ala129Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.386C>T
  hgvsp: ENSP00000442985.1:p.Ala129Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*548C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*102C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.386C>T
  hgvsp: ENSP00000450913.1:p.Ala129Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.386C>T
  hgvsp: ENSP00000452446.1:p.Ala129Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.584C>T
  hgvsp: ENSP00000352167.3:p.Ala195Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*548C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1280G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.386C>T
  hgvsp: ENSP00000452324.1:p.Ala129Val
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala195Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-100758952-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758952
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758952
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 68426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.382T>G
  hgvsp: ENSP00000452446.1:p.Leu128Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.382T>G
  hgvsp: ENSP00000442985.1:p.Leu128Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*544T>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.580T>G
  hgvsp: ENSP00000352167.3:p.Leu194Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.382T>G
  hgvsp: ENSP00000452078.1:p.Leu128Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.382T>G
  hgvsp: ENSP00000452324.1:p.Leu128Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1284A>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*98T>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*544T>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.382T>G
  hgvsp: ENSP00000450913.1:p.Leu128Val
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27499
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu194Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-100758955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758955
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758955
    reference: chr 14
allele count: 2
allele frequency: 2.901073397156948e-5
allele num: 68940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.379C>T
  hgvsp: ENST00000556505.1:c.379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.577C>T
  hgvsp: ENST00000359232.3:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.379C>T
  hgvsp: ENST00000539621.1:c.379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*541C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1287G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.379C>T
  hgvsp: ENST00000555927.1:c.379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.379C>T
  hgvsp: ENST00000554912.1:c.379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.379C>T
  hgvsp: ENST00000554291.1:c.379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*95C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*541C>T
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21663
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15887
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu193Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

14-100758960-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758960
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758960
    reference: chr 14
allele count: 3
allele frequency: 4.251700680272109e-5
allele num: 70560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*536A>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.374A>G
  hgvsp: ENSP00000452078.1:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.374A>G
  hgvsp: ENSP00000442985.1:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.572A>G
  hgvsp: ENSP00000352167.3:p.Lys191Arg
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*536A>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.374A>G
  hgvsp: ENSP00000452324.1:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.374A>G
  hgvsp: ENSP00000452446.1:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*90A>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1292T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.374A>G
  hgvsp: ENSP00000450913.1:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys191Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

14-100758962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758962
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758962
    reference: chr 14
allele count: 1
allele frequency: 1.41270872771452e-5
allele num: 70786
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.570C>T
  hgvsp: ENST00000359232.3:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.372C>T
  hgvsp: ENST00000539621.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.372C>T
  hgvsp: ENST00000556505.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.372C>T
  hgvsp: ENST00000554291.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*88C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.372C>T
  hgvsp: ENST00000554912.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1294G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*534C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*534C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.372C>T
  hgvsp: ENST00000555927.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3190
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro190Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

14-100758975-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758975
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758975
    reference: chr 14
allele count: 2
allele frequency: 3.920799843168006e-5
allele num: 51010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.359G>A
  hgvsp: ENSP00000452324.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*521G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.557G>A
  hgvsp: ENSP00000352167.3:p.Arg186His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.359G>A
  hgvsp: ENSP00000450913.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.359G>A
  hgvsp: ENSP00000452446.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.359G>A
  hgvsp: ENSP00000452078.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*521G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.359G>A
  hgvsp: ENSP00000442985.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1307C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*75G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15183
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg186His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

14-100758976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758976
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758976
    reference: chr 14
allele count: 1
allele frequency: 1.569908003391001e-5
allele num: 63698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.358C>T
  hgvsp: ENSP00000452446.1:p.Arg120Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.358C>T
  hgvsp: ENSP00000452078.1:p.Arg120Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.358C>T
  hgvsp: ENSP00000452324.1:p.Arg120Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1308G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*520C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.358C>T
  hgvsp: ENSP00000442985.1:p.Arg120Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.358C>T
  hgvsp: ENSP00000450913.1:p.Arg120Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.556C>T
  hgvsp: ENSP00000352167.3:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*74C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*520C>T
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg186Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

14-100758981-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758981
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758981
    reference: chr 14
allele count: 1
allele frequency: 1.602615468444501e-5
allele num: 62398
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.551G>C
  hgvsp: ENSP00000352167.3:p.Gly184Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.353G>C
  hgvsp: ENSP00000452078.1:p.Gly118Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*69G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.353G>C
  hgvsp: ENSP00000450913.1:p.Gly118Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*515G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.353G>C
  hgvsp: ENSP00000452446.1:p.Gly118Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*515G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1313C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.353G>C
  hgvsp: ENSP00000442985.1:p.Gly118Ala
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.353G>C
  hgvsp: ENSP00000452324.1:p.Gly118Ala
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly184Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

14-100758982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758982
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758982
    reference: chr 14
allele count: 2
allele frequency: 3.1985670419652e-5
allele num: 62528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.352G>A
  hgvsp: ENSP00000442985.1:p.Gly118Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.352G>A
  hgvsp: ENSP00000452324.1:p.Gly118Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.352G>A
  hgvsp: ENSP00000452078.1:p.Gly118Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*514G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.352G>A
  hgvsp: ENSP00000452446.1:p.Gly118Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1314C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*68G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.352G>A
  hgvsp: ENSP00000450913.1:p.Gly118Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.550G>A
  hgvsp: ENSP00000352167.3:p.Gly184Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*514G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4765
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly184Ser
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS

14-100758983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758983
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758983
    reference: chr 14
allele count: 3
allele frequency: 4.809850573975502e-5
allele num: 62372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*67G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.351G>A
  hgvsp: ENST00000539621.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*513G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.351G>A
  hgvsp: ENST00000555927.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.351G>A
  hgvsp: ENST00000556505.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.351G>A
  hgvsp: ENST00000554291.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.351G>A
  hgvsp: ENST00000554912.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*513G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1315C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.549G>A
  hgvsp: ENST00000359232.3:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro183Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

14-100758984-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758984
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758984
    reference: chr 14
allele count: 2
allele frequency: 3.224558235521733e-5
allele num: 62024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*512C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.548C>T
  hgvsp: ENSP00000352167.3:p.Pro183Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*66C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*512C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.350C>T
  hgvsp: ENSP00000452446.1:p.Pro117Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.350C>T
  hgvsp: ENSP00000450913.1:p.Pro117Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.350C>T
  hgvsp: ENSP00000452324.1:p.Pro117Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1316G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.350C>T
  hgvsp: ENSP00000442985.1:p.Pro117Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.350C>T
  hgvsp: ENSP00000452078.1:p.Pro117Leu
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6096
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro183Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-100758988-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758988
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758988
    reference: chr 14
allele count: 1
allele frequency: 1.591545709192768e-5
allele num: 62832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.346G>T
  hgvsp: ENSP00000452324.1:p.Glu116Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.346G>T
  hgvsp: ENSP00000442985.1:p.Glu116Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.346G>T
  hgvsp: ENSP00000452446.1:p.Glu116Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1320C>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*62G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.346G>T
  hgvsp: ENSP00000452078.1:p.Glu116Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*508G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.544G>T
  hgvsp: ENSP00000352167.3:p.Glu182Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.346G>T
  hgvsp: ENSP00000450913.1:p.Glu116Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*508G>T
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14551
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4659
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu182Ter
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-100758991-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758991
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758991
    reference: chr 14
allele count: 1
allele frequency: 1.581928053912108e-5
allele num: 63214
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1323A>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.541T>A
  hgvsp: ENSP00000352167.3:p.Cys181Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.343T>A
  hgvsp: ENSP00000452324.1:p.Cys115Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*505T>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.343T>A
  hgvsp: ENSP00000452078.1:p.Cys115Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*59T>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.343T>A
  hgvsp: ENSP00000450913.1:p.Cys115Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*505T>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.343T>A
  hgvsp: ENSP00000442985.1:p.Cys115Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.343T>A
  hgvsp: ENSP00000452446.1:p.Cys115Ser
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Cys181Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

14-100758993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758993
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758993
    reference: chr 14
allele count: 1
allele frequency: 1.576242867501025e-5
allele num: 63442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.341G>A
  hgvsp: ENSP00000450913.1:p.Gly114Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*57G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.341G>A
  hgvsp: ENSP00000442985.1:p.Gly114Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.539G>A
  hgvsp: ENSP00000352167.3:p.Gly180Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.341G>A
  hgvsp: ENSP00000452446.1:p.Gly114Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.341G>A
  hgvsp: ENSP00000452324.1:p.Gly114Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.341G>A
  hgvsp: ENSP00000452078.1:p.Gly114Asp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*503G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1325C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly180Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-100758998-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758998
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758998
    reference: chr 14
allele count: 1
allele frequency: 1.571931589537223e-5
allele num: 63616
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.534G>C
  hgvsp: ENST00000359232.3:c.534G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1330C>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.336G>C
  hgvsp: ENST00000556505.1:c.336G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*52G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.336G>C
  hgvsp: ENST00000554291.1:c.336G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*498G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*498G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.336G>C
  hgvsp: ENST00000539621.1:c.336G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.336G>C
  hgvsp: ENST00000555927.1:c.336G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.336G>C
  hgvsp: ENST00000554912.1:c.336G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22024
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25044
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4540
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala178Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

14-100758999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100758999
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100758999
    reference: chr 14
allele count: 2
allele frequency: 3.138337936228973e-5
allele num: 63728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.335C>T
  hgvsp: ENSP00000452078.1:p.Ala112Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.335C>T
  hgvsp: ENSP00000452446.1:p.Ala112Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.533C>T
  hgvsp: ENSP00000352167.3:p.Ala178Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.335C>T
  hgvsp: ENSP00000450913.1:p.Ala112Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.335C>T
  hgvsp: ENSP00000442985.1:p.Ala112Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*497C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.335C>T
  hgvsp: ENSP00000452324.1:p.Ala112Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*51C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*497C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1331G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4541
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24993
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala178Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

14-100759003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759003
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759003
    reference: chr 14
allele count: 1
allele frequency: 1.562646498109198e-5
allele num: 63994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.331C>T
  hgvsp: ENSP00000452078.1:p.Arg111Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.331C>T
  hgvsp: ENSP00000442985.1:p.Arg111Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*493C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.331C>T
  hgvsp: ENSP00000450913.1:p.Arg111Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*47C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.529C>T
  hgvsp: ENSP00000352167.3:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1335G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.331C>T
  hgvsp: ENSP00000452446.1:p.Arg111Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*493C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.331C>T
  hgvsp: ENSP00000452324.1:p.Arg111Trp
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg177Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

14-100759004-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759004
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759004
    reference: chr 14
allele count: 1
allele frequency: 1.547843853512058e-5
allele num: 64606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.330G>A
  hgvsp: ENST00000554291.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*46G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.528G>A
  hgvsp: ENST00000359232.3:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.330G>A
  hgvsp: ENST00000539621.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.330G>A
  hgvsp: ENST00000556505.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.330G>A
  hgvsp: ENST00000554912.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*492G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*492G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1336C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.330G>A
  hgvsp: ENST00000555927.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 22186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr176Thr
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-100759009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759009
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759009
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 65370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.325C>T
  hgvsp: ENSP00000452078.1:p.Leu109Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.325C>T
  hgvsp: ENSP00000452324.1:p.Leu109Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*41C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.325C>T
  hgvsp: ENSP00000452446.1:p.Leu109Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.325C>T
  hgvsp: ENSP00000450913.1:p.Leu109Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*487C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.325C>T
  hgvsp: ENSP00000442985.1:p.Leu109Phe
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1341G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*487C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.523C>T
  hgvsp: ENSP00000352167.3:p.Leu175Phe
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4532
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu175Phe
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

14-100759010-A-AGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759010
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759012
    reference: chr 14
allele count: 26
allele frequency: 3.962568963940622e-4
allele num: 65614
alternate allele: AGC
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*38_*39dupGC
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.322_323dupGC
  hgvsp: ENSP00000442985.1:p.Thr110SerfsTer172
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.520_521dupGC
  hgvsp: ENSP00000352167.3:p.Thr176SerfsTer172
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1344_214+1345dupCG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.322_323dupGC
  hgvsp: ENSP00000452324.1:p.Thr110SerfsTer?
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.322_323dupGC
  hgvsp: ENSP00000452078.1:p.Thr110SerfsTer?
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.322_323dupGC
  hgvsp: ENSP00000452446.1:p.Thr110SerfsTer172
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*484_*485dupGC
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.322_323dupGC
  hgvsp: ENSP00000450913.1:p.Thr110SerfsTer172
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*484_*485dupGC
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10435
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14399
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22353
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr176SerfsTer172
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

14-100759012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759012
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759012
    reference: chr 14
allele count: 2
allele frequency: 3.056795255853763e-5
allele num: 65428
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.520G>A
  hgvsp: ENSP00000352167.3:p.Ala174Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*484G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1344C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.322G>A
  hgvsp: ENSP00000452078.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.322G>A
  hgvsp: ENSP00000442985.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.322G>A
  hgvsp: ENSP00000450913.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.322G>A
  hgvsp: ENSP00000452324.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.322G>A
  hgvsp: ENSP00000452446.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*38G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*484G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22300
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14401
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala174Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

14-100759015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759015
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759015
    reference: chr 14
allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*35G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*481G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.319G>A
  hgvsp: ENSP00000442985.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1347C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.517G>A
  hgvsp: ENSP00000352167.3:p.Asp173Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.319G>A
  hgvsp: ENSP00000452324.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.319G>A
  hgvsp: ENSP00000452078.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.319G>A
  hgvsp: ENSP00000450913.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.319G>A
  hgvsp: ENSP00000452446.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*481G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14343
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp173Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-100759020-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759020
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759020
    reference: chr 14
allele count: 3
allele frequency: 4.481491440351349e-5
allele num: 66942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*476C>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.314C>A
  hgvsp: ENSP00000452446.1:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.314C>A
  hgvsp: ENSP00000452078.1:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.314C>A
  hgvsp: ENSP00000452324.1:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.314C>A
  hgvsp: ENSP00000450913.1:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.314C>A
  hgvsp: ENSP00000442985.1:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.512C>A
  hgvsp: ENSP00000352167.3:p.Thr171Asn
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*476C>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*30C>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1352G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14387
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4651
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr171Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

14-100759033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759033
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759033
    reference: chr 14
allele count: 1
allele frequency: 1.477192153155282e-5
allele num: 67696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.301G>A
  hgvsp: ENSP00000450913.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.499G>A
  hgvsp: ENSP00000352167.3:p.Val167Ile
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.301G>A
  hgvsp: ENSP00000452446.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.301G>A
  hgvsp: ENSP00000452324.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.301G>A
  hgvsp: ENSP00000452078.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*17G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.301G>A
  hgvsp: ENSP00000442985.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1365C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*463G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*463G>A
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val167Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

14-100759036-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759036
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759036
    reference: chr 14
allele count: 1
allele frequency: 1.474795740789901e-5
allele num: 67806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*460G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.298G>A
  hgvsp: ENSP00000452446.1:p.Gly100Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*14G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.298G>A
  hgvsp: ENSP00000442985.1:p.Gly100Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.298G>A
  hgvsp: ENSP00000452324.1:p.Gly100Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.496G>A
  hgvsp: ENSP00000352167.3:p.Gly166Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.298G>A
  hgvsp: ENSP00000452078.1:p.Gly100Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*460G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1368C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.298G>A
  hgvsp: ENSP00000450913.1:p.Gly100Ser
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21941
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly166Ser
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-100759036-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759036
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759036
    reference: chr 14
allele count: 2
allele frequency: 2.949591481579801e-5
allele num: 67806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.298G>T
  hgvsp: ENSP00000452324.1:p.Gly100Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*14G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.298G>T
  hgvsp: ENSP00000452446.1:p.Gly100Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*460G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.496G>T
  hgvsp: ENSP00000352167.3:p.Gly166Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.298G>T
  hgvsp: ENSP00000450913.1:p.Gly100Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.298G>T
  hgvsp: ENSP00000442985.1:p.Gly100Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.298G>T
  hgvsp: ENSP00000452078.1:p.Gly100Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*460G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1368C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21941
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8261
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5073
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly166Cys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

14-100759043-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759043
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759043
    reference: chr 14
allele count: 3
allele frequency: 4.315304948216341e-5
allele num: 69520
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.291C>T
  hgvsp: ENST00000554291.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*7C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.291C>T
  hgvsp: ENST00000554912.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.291C>T
  hgvsp: ENST00000556505.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.489C>T
  hgvsp: ENST00000359232.3:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*453C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.291C>T
  hgvsp: ENST00000539621.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*453C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.291C>T
  hgvsp: ENST00000555927.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1375G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14388
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Pro163Pro
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/14-100759046-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759046
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759046
    reference: chr 14
allele count: 52579
allele frequency: 6.059024176634631e-1
allele num: 86778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.288G>T
  hgvsp: ENST00000539621.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.288G>T
  hgvsp: ENST00000554912.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*450G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*4G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1378C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.288G>T
  hgvsp: ENST00000555927.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.486G>T
  hgvsp: ENST00000359232.3:c.486G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.288G>T
  hgvsp: ENST00000556505.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*450G>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.288G>T
  hgvsp: ENST00000554291.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.5e0
  variant carriers: 694
genotype depth: GenotypeDepth
  all individuals: 7599
  bin: 2.25e1
  variant carriers: 5642
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.25e1
  variant carriers: 763
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.25e1
  variant carriers: 455
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 363
genotype depth: GenotypeDepth
  all individuals: 16732
  bin: 1.25e1
  variant carriers: 13932
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 355
genotype depth: GenotypeDepth
  all individuals: 12679
  bin: 7.5e0
  variant carriers: 7194
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.75e1
  variant carriers: 385
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 2.75e1
  variant carriers: 2075
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 248
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 424
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 435
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 385
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 12393
  bin: 1.75e1
  variant carriers: 11384
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 434
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 415
genotype quality: GenotypeQuality
  all individuals: 6856
  bin: 2.25e1
  variant carriers: 1786
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 4.75e1
  variant carriers: 2273
hgvs: p.Thr162Thr
num of homozygotes: 15044
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

14-100759047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759047
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759047
    reference: chr 14
allele count: 1
allele frequency: 1.37544014084507e-5
allele num: 72704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*449C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.287C>T
  hgvsp: ENSP00000452078.1:p.Thr96Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.*3C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.287C>T
  hgvsp: ENSP00000452446.1:p.Thr96Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.287C>T
  hgvsp: ENSP00000452324.1:p.Thr96Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.287C>T
  hgvsp: ENSP00000450913.1:p.Thr96Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.287C>T
  hgvsp: ENSP00000442985.1:p.Thr96Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1379G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*449C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.485C>T
  hgvsp: ENSP00000352167.3:p.Thr162Met
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2812
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr162Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

14-100759053-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759053
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759053
    reference: chr 14
allele count: 1
allele frequency: 1.4027999887776e-5
allele num: 71286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.281G>A
  hgvsp: ENSP00000452078.1:p.Arg94His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.479G>A
  hgvsp: ENSP00000352167.3:p.Arg160His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1385C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.281G>A
  hgvsp: ENSP00000442985.1:p.Arg94His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*443G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.281G>A
  hgvsp: ENSP00000452324.1:p.Arg94His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.281G>A
  hgvsp: ENSP00000452446.1:p.Arg94His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*443G>A
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.281G>A
  hgvsp: ENSP00000450913.1:p.Arg94His
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.435G>A
  hgvsp: ENST00000392908.3:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16677
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4241
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg160His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

14-100759062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759062
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759062
    reference: chr 14
allele count: 1
allele frequency: 1.426818480152955e-5
allele num: 70086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*434C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.272C>T
  hgvsp: ENSP00000452324.1:p.Thr91Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.272C>T
  hgvsp: ENSP00000452078.1:p.Thr91Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.272C>T
  hgvsp: ENSP00000442985.1:p.Thr91Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.272C>T
  hgvsp: ENSP00000452446.1:p.Thr91Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.272C>T
  hgvsp: ENSP00000450913.1:p.Thr91Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*434C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.470C>T
  hgvsp: ENSP00000352167.3:p.Thr157Met
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.426C>T
  hgvsp: ENST00000392908.3:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1394G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10235
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr157Met
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

14-100759078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759078
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759078
    reference: chr 14
allele count: 2
allele frequency: 2.964544053124629e-5
allele num: 67464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.256C>T
  hgvsp: ENSP00000442985.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.410C>T
  hgvsp: ENSP00000451644.1:p.Pro137Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.454C>T
  hgvsp: ENSP00000352167.3:p.Arg152Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.256C>T
  hgvsp: ENSP00000452446.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.256C>T
  hgvsp: ENSP00000450913.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*418C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.256C>T
  hgvsp: ENSP00000452078.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*418C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1410G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.410C>T
  hgvsp: ENSP00000376640.3:p.Pro137Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.256C>T
  hgvsp: ENSP00000452324.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16436
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg152Trp
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

14-100759079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759079
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759079
    reference: chr 14
allele count: 1
allele frequency: 1.481086525074795e-5
allele num: 67518
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1411G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*417C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.255C>T
  hgvsp: ENST00000554912.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.409C>T
  hgvsp: ENSP00000376640.3:p.Pro137Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*417C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.453C>T
  hgvsp: ENST00000359232.3:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.409C>T
  hgvsp: ENSP00000451644.1:p.Pro137Ser
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.255C>T
  hgvsp: ENST00000554291.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.255C>T
  hgvsp: ENST00000555927.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.255C>T
  hgvsp: ENST00000539621.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.255C>T
  hgvsp: ENST00000556505.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22102
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro137Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

14-100759085-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759085
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759085
    reference: chr 14
allele count: 7
allele frequency: 1.052473312283867e-4
allele num: 66510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.403C>T
  hgvsp: ENSP00000451644.1:p.Arg135Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.249C>T
  hgvsp: ENST00000539621.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*411C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.249C>T
  hgvsp: ENST00000555927.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.249C>T
  hgvsp: ENST00000554291.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1417G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.447C>T
  hgvsp: ENST00000359232.3:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.249C>T
  hgvsp: ENST00000556505.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.403C>T
  hgvsp: ENSP00000376640.3:p.Arg135Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.249C>T
  hgvsp: ENST00000554912.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*411C>T
  variant of: http://identifiers.org/hgnc/20116
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16447
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg135Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-100759088-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759088
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759088
    reference: chr 14
allele count: 54
allele frequency: 8.125188083057478e-4
allele num: 66460
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.246T>G
  hgvsp: ENST00000555927.1:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.246T>G
  hgvsp: ENST00000554291.1:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*408T>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.246T>G
  hgvsp: ENST00000539621.1:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*408T>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.400T>G
  hgvsp: ENSP00000451644.1:p.Trp134Gly
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1420A>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.246T>G
  hgvsp: ENST00000554912.1:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.444T>G
  hgvsp: ENST00000359232.3:c.444T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.400T>G
  hgvsp: ENSP00000376640.3:p.Trp134Gly
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.246T>G
  hgvsp: ENST00000556505.1:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16481
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7504
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22444
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp134Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

14-100759090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759090
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759090
    reference: chr 14
allele count: 175
allele frequency: 2.661758890274694e-3
allele num: 65746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*406C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.244C>T
  hgvsp: ENSP00000452446.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.244C>T
  hgvsp: ENSP00000452078.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.244C>T
  hgvsp: ENSP00000442985.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.244C>T
  hgvsp: ENSP00000452324.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*406C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.398C>T
  hgvsp: ENSP00000451644.1:p.Ala133Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.442C>T
  hgvsp: ENSP00000352167.3:p.Arg148Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.398C>T
  hgvsp: ENSP00000376640.3:p.Ala133Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.244C>T
  hgvsp: ENSP00000450913.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1422G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 2.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 22442
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16549
  bin: 1.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 1.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg148Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

14-100759099-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759099
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759099
    reference: chr 14
allele count: 1
allele frequency: 1.547412725922258e-5
allele num: 64624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.389G>C
  hgvsp: ENSP00000376640.3:p.Arg130Pro
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.235G>C
  hgvsp: ENSP00000452446.1:p.Glu79Gln
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.235G>C
  hgvsp: ENSP00000442985.1:p.Glu79Gln
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.235G>C
  hgvsp: ENSP00000452078.1:p.Glu79Gln
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*397G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.389G>C
  hgvsp: ENSP00000451644.1:p.Arg130Pro
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*397G>C
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.235G>C
  hgvsp: ENSP00000452324.1:p.Glu79Gln
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.235G>C
  hgvsp: ENSP00000450913.1:p.Glu79Gln
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.433G>C
  hgvsp: ENSP00000352167.3:p.Glu145Gln
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1431C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu145Gln
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

14-100759100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759100
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759100
    reference: chr 14
allele count: 1
allele frequency: 1.549138678894535e-5
allele num: 64552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*396C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.234C>T
  hgvsp: ENST00000554912.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.432C>T
  hgvsp: ENST00000359232.3:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.388C>T
  hgvsp: ENSP00000376640.3:p.Arg130Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*396C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1432G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.234C>T
  hgvsp: ENST00000556505.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.388C>T
  hgvsp: ENSP00000451644.1:p.Arg130Ter
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.234C>T
  hgvsp: ENST00000539621.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.234C>T
  hgvsp: ENST00000555927.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.234C>T
  hgvsp: ENST00000554291.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg130Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

14-100759102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759102
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759102
    reference: chr 14
allele count: 1
allele frequency: 1.553615262716341e-5
allele num: 64366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.232C>T
  hgvsp: ENSP00000452446.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.232C>T
  hgvsp: ENSP00000450913.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.386C>T
  hgvsp: ENSP00000451644.1:p.Ala129Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*394C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.232C>T
  hgvsp: ENSP00000442985.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.430C>T
  hgvsp: ENSP00000352167.3:p.His144Tyr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.232C>T
  hgvsp: ENSP00000452324.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.386C>T
  hgvsp: ENSP00000376640.3:p.Ala129Val
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1434G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*394C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.232C>T
  hgvsp: ENSP00000452078.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His144Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-100759106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759106
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759106
    reference: chr 14
allele count: 2
allele frequency: 3.17299149638279e-5
allele num: 63032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.228C>T
  hgvsp: ENST00000554291.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.382C>T
  hgvsp: ENSP00000451644.1:p.Arg128Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.426C>T
  hgvsp: ENST00000359232.3:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*390C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.228C>T
  hgvsp: ENST00000556505.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.382C>T
  hgvsp: ENSP00000376640.3:p.Arg128Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.228C>T
  hgvsp: ENST00000539621.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.228C>T
  hgvsp: ENST00000554912.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.228C>T
  hgvsp: ENST00000555927.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1438G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*390C>T
  variant of: http://identifiers.org/hgnc/20116
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22850
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg128Trp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

14-100759124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759124
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759124
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 60152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*372C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.364C>T
  hgvsp: ENST00000392908.3:c.364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.210C>T
  hgvsp: ENST00000554291.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.408C>T
  hgvsp: ENST00000359232.3:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.210C>T
  hgvsp: ENST00000539621.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451808
  ensembl transcript: ENST00000556868
  gene symbol: SLC25A29
  hgvsc: ENST00000556868.1:c.*407C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.210C>T
  hgvsp: ENST00000555927.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.210C>T
  hgvsp: ENST00000554912.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*372C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.210C>T
  hgvsp: ENST00000556505.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1456G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.364C>T
  hgvsp: ENST00000554060.1:c.364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp136Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-100759131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759131
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759131
    reference: chr 14
allele count: 4
allele frequency: 6.841583142339137e-5
allele num: 58466
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1463G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*365C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*365C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451808
  ensembl transcript: ENST00000556868
  gene symbol: SLC25A29
  hgvsc: ENST00000556868.1:c.*400C>T
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.357C>T
  hgvsp: ENST00000392908.3:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.401C>T
  hgvsp: ENSP00000352167.3:p.Ser134Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.203C>T
  hgvsp: ENSP00000452078.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.203C>T
  hgvsp: ENSP00000452324.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.203C>T
  hgvsp: ENSP00000450913.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.203C>T
  hgvsp: ENSP00000452446.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.357C>T
  hgvsp: ENST00000554060.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.203C>T
  hgvsp: ENSP00000442985.1:p.Ser68Leu
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23366
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17625
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser134Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

14-100759131-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100759131
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100759131
    reference: chr 14
allele count: 1
allele frequency: 1.710395785584784e-5
allele num: 58466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451952
  ensembl transcript: ENST00000556715
  gene symbol: SLC25A29
  hgvsc: ENST00000556715.2:c.*365C>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452446
  ensembl transcript: ENST00000556505
  gene symbol: SLC25A29
  hgvsc: ENST00000556505.1:c.203C>G
  hgvsp: ENSP00000452446.1:p.Ser68Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000450913
  ensembl transcript: ENST00000554912
  gene symbol: SLC25A29
  hgvsc: ENST00000554912.1:c.203C>G
  hgvsp: ENSP00000450913.1:p.Ser68Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451808
  ensembl transcript: ENST00000556868
  gene symbol: SLC25A29
  hgvsc: ENST00000556868.1:c.*400C>G
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258504
  ensembl transcript: ENST00000556458
  gene symbol: RP11-638I2.6
  hgvsc: ENST00000556458.1:n.214+1463G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451644
  ensembl transcript: ENST00000554060
  gene symbol: SLC25A29
  hgvsc: ENST00000554060.1:c.357C>G
  hgvsp: ENST00000554060.1:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000352167
  ensembl transcript: ENST00000359232
  gene symbol: SLC25A29
  hgvsc: ENST00000359232.3:c.401C>G
  hgvsp: ENSP00000352167.3:p.Ser134Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000442985
  ensembl transcript: ENST00000539621
  gene symbol: SLC25A29
  hgvsc: ENST00000539621.1:c.203C>G
  hgvsp: ENSP00000442985.1:p.Ser68Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000376640
  ensembl transcript: ENST00000392908
  gene symbol: SLC25A29
  hgvsc: ENST00000392908.3:c.357C>G
  hgvsp: ENST00000392908.3:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452078
  ensembl transcript: ENST00000555927
  gene symbol: SLC25A29
  hgvsc: ENST00000555927.1:c.203C>G
  hgvsp: ENSP00000452078.1:p.Ser68Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000452324
  ensembl transcript: ENST00000554291
  gene symbol: SLC25A29
  hgvsc: ENST00000554291.1:c.203C>G
  hgvsp: ENSP00000452324.1:p.Ser68Trp
  variant of: http://identifiers.org/hgnc/20116
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197119
  ensembl protein: ENSP00000451573
  ensembl transcript: ENST00000554224
  gene symbol: SLC25A29
  hgvsc: ENST00000554224.1:c.*365C>G
  variant of: http://identifiers.org/hgnc/20116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser134Trp
num of homozygotes: 0
population: African
reference allele: G

GenotypeQuality
all individuals: 2153
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2250
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31292
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2192
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.21e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.038e1

DP
type: SiteQuality
SIO_000300: 5.64984e5

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

VQSLOD
type: SiteQuality
SIO_000300: -4.225e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6483
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9799
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31441
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 79
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1986
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.118318049653321e-4
allele num: 17884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.051e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

FS
type: SiteQuality
SIO_000300: 1.249e0

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 7.04e0

DP
type: SiteQuality
SIO_000300: 5.67919e5

GenotypeQuality
all individuals: 23
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 822
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 568
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 168
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.11000111000111e-4
allele num: 18018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.14e-2

DP
type: SiteQuality
SIO_000300: 5.68381e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

FS
type: SiteQuality
SIO_000300: 1.348e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2962
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.108524553818867e-4
allele num: 18042
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.74e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

DP
type: SiteQuality
SIO_000300: 5.67555e5

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 3.653e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 58

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3004
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 1.181102362204724e-2
allele num: 254
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.241090146750524e-4
allele num: 1908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 2.346905359676891e-3
allele num: 18322
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.277955271565495e-2
allele num: 626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2310
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.064282673478076e-4
allele num: 9396
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

DP
type: SiteQuality
SIO_000300: 5.68748e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.184e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1980
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.367686527106817e-5
allele num: 18630
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

DP
type: SiteQuality
SIO_000300: 5.73286e5

FS
type: SiteQuality
SIO_000300: 5.012e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.044168319933173e-4
allele num: 19154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3052
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.049758555532228e-4
allele num: 9526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2070
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.7354e1

DP
type: SiteQuality
SIO_000300: 5.7962e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.05e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.544e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

African
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allele count: 1
allele frequency: 3.250975292587776e-4
allele num: 3076
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

FS
type: SiteQuality
SIO_000300: 6.286e0

DP
type: SiteQuality
SIO_000300: 5.82649e5

QD
type: SiteQuality
SIO_000300: 1.031e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.93e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.926593753079121e-5
allele num: 20298
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-1

FS
type: SiteQuality
SIO_000300: 8.378e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.90431e5

MQ
type: SiteQuality
SIO_000300: 5.338e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.243e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

QD
type: SiteQuality
SIO_000300: 2.31e0

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
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 4.310344827586207e-4
allele num: 2320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.878524734120402e-5
allele num: 20498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2524
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VQSLOD
type: SiteQuality
SIO_000300: 6.79e-1

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.178e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.201e0

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 267
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GenotypeQuality
all individuals: 2460
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3224
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.803996925441968e-5
allele num: 20816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
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VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 5.99129e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

QD
type: SiteQuality
SIO_000300: 7.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.73305566073457e-5
allele num: 21128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2594
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.03817e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.55e-1

VQSLOD
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SIO_000300: -2.298e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.76e-2

FS
type: SiteQuality
SIO_000300: 7.204e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.164e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.513450081242101e-5
allele num: 22156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.16557e5

FS
type: SiteQuality
SIO_000300: 2.908e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.219e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.89e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 916
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.449e0

VQSLOD
type: SiteQuality
SIO_000300: -1.015e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.63e-2

MQ
type: SiteQuality
SIO_000300: 5.79e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

DP
type: SiteQuality
SIO_000300: 6.42061e5

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

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3610
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.360215053763441e-4
allele num: 2976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24004
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.583e0

QD
type: SiteQuality
SIO_000300: 6.99e0

VQSLOD
type: SiteQuality
SIO_000300: -3.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

DP
type: SiteQuality
SIO_000300: 6.47254e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 86
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.817396426467701e-5
allele num: 10186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3060
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.33e0

QD
type: SiteQuality
SIO_000300: 1.27e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.281e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.49e-2

DP
type: SiteQuality
SIO_000300: 6.52769e5

FS
type: SiteQuality
SIO_000300: 2.566e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26262
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 1.778e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

DP
type: SiteQuality
SIO_000300: 6.84598e5

FS
type: SiteQuality
SIO_000300: 5.193e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.091861988644635e-4
allele num: 27476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10570
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.1e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.98099e5

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.029866117404737e-4
allele num: 29130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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Latino
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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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bin: 4.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.297016861219196e-4
allele num: 30840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4482
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1480
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

FS
type: SiteQuality
SIO_000300: 8.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.181e1

DP
type: SiteQuality
SIO_000300: 7.36923e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 4.899559039686428e-4
allele num: 4082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.295e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.40768e5

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.420545746388443e-5
allele num: 31150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3956
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.13e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

DP
type: SiteQuality
SIO_000300: 7.4059e5

FS
type: SiteQuality
SIO_000300: 7.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e0

QD
type: SiteQuality
SIO_000300: 7.73e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31348
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.005763688760806e-5
allele num: 11104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3990
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.42998e5

FS
type: SiteQuality
SIO_000300: 4.752e0

VQSLOD
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

QD
type: SiteQuality
SIO_000300: 1.505e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.203e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.099420555047271e-5
allele num: 32790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.50929e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.868e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.91e-1

QD
type: SiteQuality
SIO_000300: 1.119e1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.049710277523635e-5
allele num: 32790
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.87941751021133e-5
allele num: 11262
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

DP
type: SiteQuality
SIO_000300: 7.50929e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.91e-1

FS
type: SiteQuality
SIO_000300: 1.868e0

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

QD
type: SiteQuality
SIO_000300: 1.119e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4386
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.77683013503909e-4
allele num: 11256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.237e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.29e0

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

East Asian
type: Population
allele count: 1
allele frequency: 2.092925910422771e-4
allele num: 4778
num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2012
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Latino
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.444547285893178e-5
allele num: 36734
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.263e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.22831e5

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 5290
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4926
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38202
num of homozygotes: 0

QD
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SIO_000300: 6.31e0

FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
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SIO_000300: -1.438e0

DP
type: SiteQuality
SIO_000300: 8.35201e5

BaseQRankSum
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SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 5.739e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 4960
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12026
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 5.193995740923493e-5
allele num: 38506
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2202
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
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InbreedingCoeff
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MQRankSum
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SIO_000300: 2.62e-1

DP
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BaseQRankSum
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SIO_000300: -2.269e0

MQ
type: SiteQuality
SIO_000300: 5.824e1

FS
type: SiteQuality
SIO_000300: 1.972e0

VQSLOD
type: SiteQuality
SIO_000300: -2.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 7.592245786303589e-5
allele num: 39514
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2288
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5414
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12132
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.824e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.01e-2

MQRankSum
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SIO_000300: -8.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

BaseQRankSum
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SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.50953e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5078
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2312
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.843657817109145e-4
allele num: 5424
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.96e-1

DP
type: SiteQuality
SIO_000300: 8.48178e5

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.377e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.502e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1108
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.964129135113592e-5
allele num: 10036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.35795836131632e-5
allele num: 29780
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3226
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.63072e2

BaseQRankSum
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SIO_000300: -1.532e0

DP
type: SiteQuality
SIO_000300: 7.45464e5

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

ClippingRankSum
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SIO_000300: 1.21e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 4684
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4454
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 35972
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 8.77963125548727e-5
allele num: 11390
num of homozygotes: 0

MQRankSum
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SIO_000300: 7.41e-1

MQ
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DP
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1966
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.828214265512755e-5
allele num: 35358
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 0.0e0
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African
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South Asian
type: Population
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Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.17218e5

VQSLOD
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InbreedingCoeff
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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QD
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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Other
type: Population
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 5.645571049511658e-5
allele num: 35426
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2056
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.296738631143776e-4
allele num: 4354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.831577755125156e-5
allele num: 35316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4448
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.917424647761727e-5
allele num: 11214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.20341e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.25e-2

QD
type: SiteQuality
SIO_000300: 9.84e0

FS
type: SiteQuality
SIO_000300: 6.263e0

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.208e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.668291576918717e-5
allele num: 35284
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11200
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 9.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.22397e5

FS
type: SiteQuality
SIO_000300: 1.7321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4586
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.901548869503294e-5
allele num: 11234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.2601e1

QD
type: SiteQuality
SIO_000300: 7.07e0

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.485e0

InbreedingCoeff
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SIO_000300: -1.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.707e0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.097e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4480
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.844861135680169e-5
allele num: 11306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1902
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35942
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.32895e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

MQ
type: SiteQuality
SIO_000300: 5.788e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.196e0

VQSLOD
type: SiteQuality
SIO_000300: -3.281e0

QD
type: SiteQuality
SIO_000300: 1.4e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35916
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.852691218130312e-5
allele num: 11296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4562
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

FS
type: SiteQuality
SIO_000300: 2.003e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.154e0

DP
type: SiteQuality
SIO_000300: 7.3499e5

QD
type: SiteQuality
SIO_000300: 1.216e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.182453077258839e-4
allele num: 4582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4672
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36032
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2120
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.40163e5

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.671e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: -1.369e0

FS
type: SiteQuality
SIO_000300: 2.522e0

QD
type: SiteQuality
SIO_000300: 9.68e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.768242719521648e-5
allele num: 36124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 4.930966469428008e-4
allele num: 2028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4506
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FS
type: SiteQuality
SIO_000300: 2.09e0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.81e-1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.756187641254617e-5
allele num: 36282
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1912
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 418
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MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.216e0

DP
type: SiteQuality
SIO_000300: 7.5012e5

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

ClippingRankSum
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QD
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ReadPosRankSum
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SIO_000300: 1.27e0

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 2184
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4720
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European (Non-Finnish)
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allele frequency: 2.739275735495535e-5
allele num: 36506
num of homozygotes: 0

DP
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SIO_000300: 7.52625e5

QD
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InbreedingCoeff
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SIO_000300: -1.1e-2

MQRankSum
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FS
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

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

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

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

East Asian
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allele frequency: 0.0e0
allele num: 4610
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36980
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

African
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.01e-2

QD
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DP
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MQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

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

European (Non-Finnish)
type: Population
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allele frequency: 4.307095940562076e-4
allele num: 37148
num of homozygotes: 0

South Asian
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allele frequency: 6.063756063756063e-4
allele num: 11544
num of homozygotes: 1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 2
allele frequency: 4.111842105263158e-4
allele num: 4864
num of homozygotes: 0

African
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allele frequency: 2.070393374741201e-4
allele num: 4830
num of homozygotes: 0

DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.019e1

FS
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.885e1

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

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

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

South Asian
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allele frequency: 1.735207357279195e-4
allele num: 11526
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 2.212e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ReadPosRankSum
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SIO_000300: 4.06e-1

QD
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InbreedingCoeff
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SIO_000300: -1.09e-2

ClippingRankSum
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SIO_000300: -4.15e-1

BaseQRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 7.78e-1

MQ
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SIO_000300: 6.0e1

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

European (Non-Finnish)
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allele frequency: 2.669371629918317e-5
allele num: 37462
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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DP
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QD
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MQ
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
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Latino
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allele num: 5052
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European (Non-Finnish)
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allele count: 2
allele frequency: 5.284574327537916e-5
allele num: 37846
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38192
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 8.528057308545113e-5
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Other
type: Population
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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VQSLOD
type: SiteQuality
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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East Asian
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Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38236
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.899696048632219e-4
allele num: 5264
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.729e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

MQ
type: SiteQuality
SIO_000300: 5.871e1

FS
type: SiteQuality
SIO_000300: 2.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

QD
type: SiteQuality
SIO_000300: 4.76e0

DP
type: SiteQuality
SIO_000300: 7.80651e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.508e0

GenotypeQuality
all individuals: 230
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23432
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3873
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4432
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1176
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.230672664504655e-5
allele num: 38236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11734
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

DP
type: SiteQuality
SIO_000300: 7.80651e5

VQSLOD
type: SiteQuality
SIO_000300: -9.729e-1

FS
type: SiteQuality
SIO_000300: 2.83e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.508e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 4.76e0

GenotypeQuality
all individuals: 298
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4353
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23581
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 7.25e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4984
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 5.841121495327102e-4
allele num: 5136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39100
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

DP
type: SiteQuality
SIO_000300: 7.96662e5

QD
type: SiteQuality
SIO_000300: 1.026e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 995
bin: 5.75e1
variant carriers: 932

GenotypeQuality
all individuals: 1488
bin: 7.5e0
variant carriers: 548

GenotypeQuality
all individuals: 826
bin: 7.75e1
variant carriers: 805

GenotypeQuality
all individuals: 919
bin: 1.25e1
variant carriers: 624

GenotypeQuality
all individuals: 2087
bin: 5.25e1
variant carriers: 1930

GenotypeQuality
all individuals: 2333
bin: 2.5e0
variant carriers: 241

GenotypeQuality
all individuals: 572
bin: 7.25e1
variant carriers: 535

GenotypeQuality
all individuals: 747
bin: 9.25e1
variant carriers: 747

GenotypeQuality
all individuals: 783
bin: 8.25e1
variant carriers: 777

GenotypeQuality
all individuals: 2909
bin: 3.25e1
variant carriers: 2339

GenotypeQuality
all individuals: 1241
bin: 6.75e1
variant carriers: 1048

GenotypeQuality
all individuals: 1516
bin: 4.25e1
variant carriers: 1390

GenotypeQuality
all individuals: 787
bin: 8.75e1
variant carriers: 787

GenotypeQuality
all individuals: 1868
bin: 2.75e1
variant carriers: 1197

GenotypeQuality
all individuals: 1712
bin: 1.75e1
variant carriers: 1270

GenotypeQuality
all individuals: 23219
bin: 9.75e1
variant carriers: 23219

GenotypeQuality
all individuals: 2743
bin: 3.75e1
variant carriers: 2432

GenotypeQuality
all individuals: 3624
bin: 6.25e1
variant carriers: 1347

African
type: Population
allele count: 3177
allele frequency: 4.922528664394174e-1
allele num: 6454
num of homozygotes: 682

European (Non-Finnish)
type: Population
allele count: 28954
allele frequency: 6.056308567603749e-1
allele num: 47808
num of homozygotes: 8115

European (Finnish)
type: Population
allele count: 2618
allele frequency: 6.907651715039578e-1
allele num: 3790
num of homozygotes: 824

East Asian
type: Population
allele count: 4856
allele frequency: 7.463879495849984e-1
allele num: 6506
num of homozygotes: 1734

Other
type: Population
allele count: 326
allele frequency: 5.582191780821918e-1
allele num: 584
num of homozygotes: 81

Latino
type: Population
allele count: 5870
allele frequency: 7.122057752972579e-1
allele num: 8242
num of homozygotes: 1965

South Asian
type: Population
allele count: 6778
allele frequency: 5.060474839480364e-1
allele num: 13394
num of homozygotes: 1643

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.62e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.083241e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 2.193e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

GenotypeQuality
all individuals: 1796
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2887
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23990
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4789
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5268
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.276775368316503e-5
allele num: 12082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

QD
type: SiteQuality
SIO_000300: 1.762e1

FS
type: SiteQuality
SIO_000300: 5.994e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: -1.284e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.184e0

DP
type: SiteQuality
SIO_000300: 8.13867e5

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1739
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 3534
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4676
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 4.0290088638195e-4
allele num: 2482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11974
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.833e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.256e0

FS
type: SiteQuality
SIO_000300: 1.348e0

QD
type: SiteQuality
SIO_000300: 1.609e1

DP
type: SiteQuality
SIO_000300: 8.07071e5

GenotypeQuality
all individuals: 3695
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4400
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4254
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 26686
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2490
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38804
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.397715821296607e-5
allele num: 11908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2360
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.357e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

FS
type: SiteQuality
SIO_000300: 8.659000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

DP
type: SiteQuality
SIO_000300: 8.02517e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4053
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
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variant carriers: 0

GenotypeQuality
all individuals: 1397
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variant carriers: 0

GenotypeQuality
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 27916
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4189
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.75e1
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GenotypeQuality
all individuals: 215
bin: 5.75e1
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GenotypeQuality
all individuals: 4050
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 803
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10119
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.689328743545611e-5
allele num: 37184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2188
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.972386587771203e-4
allele num: 5070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

FS
type: SiteQuality
SIO_000300: 6.258e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 6.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

DP
type: SiteQuality
SIO_000300: 7.88634e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.076e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
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variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4069
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 1

GenotypeQuality
all individuals: 199
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variant carriers: 0

GenotypeQuality
all individuals: 28100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10064
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variant carriers: 0

GenotypeQuality
all individuals: 610
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variant carriers: 0

GenotypeQuality
all individuals: 1366
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variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1094
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4192
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.687016337059329e-5
allele num: 37216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4770
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
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SIO_000300: 4.12e0

VQSLOD
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SIO_000300: -2.062e0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -3.52e-1

DP
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SIO_000300: 7.85976e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

FS
type: SiteQuality
SIO_000300: 4.133e0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 312
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.72881078426022e-5
allele num: 36646
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 5.137866072957698e-4
allele num: 11678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 1.04e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

DP
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SIO_000300: 7.79818e5

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 3.351e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.13e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 90
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variant carriers: 3

GenotypeQuality
all individuals: 1746
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 9.407337723424271e-4
allele num: 2126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 1.393290350781335e-3
allele num: 36604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.012072434607646e-4
allele num: 4970
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.122e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.78e-1

DP
type: SiteQuality
SIO_000300: 7.76196e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.222e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
all individuals: 1645
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 167

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 307
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GenotypeQuality
all individuals: 640
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 34
allele frequency: 1.63147792706334e-2
allele num: 2084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 135
allele frequency: 3.730518403890793e-3
allele num: 36188
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.69434090138936e-4
allele num: 5902
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 8.183306055646482e-4
allele num: 4888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.59697386519945e-5
allele num: 11632
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.47e-1

FS
type: SiteQuality
SIO_000300: 1.097e0

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

QD
type: SiteQuality
SIO_000300: 1.25e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

DP
type: SiteQuality
SIO_000300: 7.71815e5

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 224
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
all individuals: 297
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1962
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.811041772080733e-5
allele num: 35574
num of homozygotes: 0

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

African
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allele count: 0
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BaseQRankSum
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SIO_000300: -2.331e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-1

MQ
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FS
type: SiteQuality
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

QD
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1958
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 35522
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -4.2e-1

InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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FS
type: SiteQuality
SIO_000300: 9.63e-1

BaseQRankSum
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MQRankSum
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SIO_000300: 1.19e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 389
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35410
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4484
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 2.091175240485153e-4
allele num: 4782
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South Asian
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8342
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GenotypeQuality
all individuals: 74
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.885503231763619e-5
allele num: 34656
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.756234632946962e-4
allele num: 5694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1876
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.42944e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

QD
type: SiteQuality
SIO_000300: 5.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.581e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.28e-2

FS
type: SiteQuality
SIO_000300: 3.48e0

MQRankSum
type: SiteQuality
SIO_000300: 5.04e-1

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6519
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4067
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1592
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11184
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 1.142e0

DP
type: SiteQuality
SIO_000300: 6.98937e5

QD
type: SiteQuality
SIO_000300: 7.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.52e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.485e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeDepth
all individuals: 3874
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 450
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1827
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2268
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7040
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5592
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 70
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.247660636306925e-4
allele num: 32060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11052
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

FS
type: SiteQuality
SIO_000300: 5.088e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.116e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

DP
type: SiteQuality
SIO_000300: 6.82635e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2268
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1827
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7040
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5592
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4169
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.387774594078319e-4
allele num: 4188
num of homozygotes: 0