17-79872369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872369
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872369
    reference: chr 17
allele count: 1
allele frequency: 8.310893919750009e-6
allele num: 120324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.574G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.199G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.617G>A
  hgvsp: ENSP00000329466.6:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.571G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.721G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.733G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.170G>A
  hgvsp: ENSP00000461044.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*348G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.234G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1223G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.481G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1448G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1727G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.586G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23356
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg206Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

17-79872373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872373
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872373
    reference: chr 17
allele count: 1
allele frequency: 8.308960382876895e-6
allele num: 120352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.230G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1723G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.477G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.567G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1219G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.582G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.570G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.166G>A
  hgvsp: ENSP00000461044.1:p.Val56Met
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.729G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1444G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.717G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.613G>A
  hgvsp: ENSP00000329466.6:p.Val205Met
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.195G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*344G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9035
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val205Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-79872381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872381
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872381
    reference: chr 17
allele count: 1
allele frequency: 8.307717869901138e-6
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.721G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.469G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.605G>A
  hgvsp: ENSP00000329466.6:p.Arg202Lys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.559G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1211G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-1G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.158G>A
  hgvsp: ENSP00000461044.1:p.Arg53Lys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.709G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.574G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.562G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.187G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.222G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*336G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1436G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.1716-1G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

17-79872383-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872383
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872383
    reference: chr 17
allele count: 1
allele frequency: 8.307579835842223e-6
allele num: 120372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.185C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.560C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.156C>A
  hgvsp: ENSP00000461044.1:p.Asn52Lys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*334C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1434C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.467C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.603C>A
  hgvsp: ENSP00000329466.6:p.Asn201Lys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-3C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.557C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.220C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.719C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.707C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.572C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1209C>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn201Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

17-79872391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872391
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872391
    reference: chr 17
allele count: 49
allele frequency: 4.070443595281608e-4
allele num: 120380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.595G>A
  hgvsp: ENSP00000329466.6:p.Val199Ile
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.699G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.564G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.148G>A
  hgvsp: ENSP00000461044.1:p.Val50Ile
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-11G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.212G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*326G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.549G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.552G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1201G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.711G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.177G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1426G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.459G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23376
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val199Ile
num of homozygotes: 1
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

17-79872392-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872392
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872392
    reference: chr 17
allele count: 3
allele frequency: 2.492315360970341e-5
allele num: 120370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.563C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.710C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.147C>T
  hgvsp: ENST00000572902.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.176C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.458C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*325C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.698C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.548C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.211C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.594C>T
  hgvsp: ENST00000328666.6:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-12C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.551C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1425C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1200C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys198Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

17-79872396-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872396
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872396
    reference: chr 17
allele count: 5
allele frequency: 4.15337586390218e-5
allele num: 120384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-16C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*321C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.559C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.172C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.547C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.590C>G
  hgvsp: ENSP00000329466.6:p.Ser197Cys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1421C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1196C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.143C>G
  hgvsp: ENSP00000461044.1:p.Ser48Cys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.454C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.694C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.544C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.706C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.207C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser197Cys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

17-79872412-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872412
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872412
    reference: chr 17
allele count: 2
allele frequency: 1.661239949498306e-5
allele num: 120392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-32C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-6C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-6C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-6C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.543C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-6C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.191C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.678C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.156C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1180C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1405C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-6C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-6C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-6C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.580-6C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

17-79872413-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872413
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872413
    reference: chr 17
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-33C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-7C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.542C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-7C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1404C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-7C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.155C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-7C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.677C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-7C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-7C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-7C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1179C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.190C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.580-7C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

17-79872415-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872415
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872415
    reference: chr 17
allele count: 1
allele frequency: 8.306475728477921e-6
allele num: 120388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-9T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.675T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1402T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-9T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-9T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-9T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-9T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-35T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-9T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.188T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.153T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1177T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.540T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-9T>C
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

17-79872420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872420
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872420
    reference: chr 17
allele count: 12
allele frequency: 9.969095803010666e-5
allele num: 120372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.670C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.183C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-14C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.148C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.535C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-14C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-14C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1172C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-14C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-14C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1397C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1716-40C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-14C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-14C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-79872435-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872435
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872435
    reference: chr 17
allele count: 2
allele frequency: 1.662786830728301e-5
allele num: 120280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-29T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-29T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-29T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.520T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-29T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.133T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1382T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1157T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-29T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-29T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.168T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+45T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-29T>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.655T>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9038
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

17-79872436-C-CGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872436
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872438
    reference: chr 17
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: CGT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.166_167insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.131_132insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-31_580-30insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-31_133-30insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-31_444-30insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-31_696-30insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1380_1381insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+43_1715+44insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-31_537-30insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.518_519insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.653_654insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1155_1156insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-31_534-30insAC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-31_*311-30insAC
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

17-79872437-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872437
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872437
    reference: chr 17
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1380G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+43G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-31G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.518G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.166G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-31G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-31G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-31G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.131G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1155G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-31G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.653G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-31G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-31G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

17-79872439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872439
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872439
    reference: chr 17
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1153C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.516C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-33C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-33C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.164C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.129C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-33C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1378C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.651C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-33C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-33C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-33C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+41C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-33C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

17-79872442-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872442
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872442
    reference: chr 17
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.513A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.648A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.126A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.444-36A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1375A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.133-36A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1150A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.161A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*311-36A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+38A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.696-36A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.534-36A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.537-36A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.580-36A>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-79872449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872449
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872449
    reference: chr 17
allele count: 1
allele frequency: 8.305371914554334e-6
allele num: 120404
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.579+31C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.132+31C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.533+31C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1143C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.695+31C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.506C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+31C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.154C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.641C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.536+31C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1368C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.443+31C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.119C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*310+31C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14975
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-79872463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872463
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872463
    reference: chr 17
allele count: 1
allele frequency: 8.306337735692333e-6
allele num: 120390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.132+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.492G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.140G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.536+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.579+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.695+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.627G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1354G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*310+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.443+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.533+17G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1129G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.105G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

17-79872465-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872465
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872466
    reference: chr 17
allele count: 1
allele frequency: 8.306613725848521e-6
allele num: 120386
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1126dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.624dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.137dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*310+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.533+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1351dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.695+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.443+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.489dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.536+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.579+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.132+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+14dupC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.102dupC
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

17-79872468-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872468
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872468
    reference: chr 17
allele count: 2
allele frequency: 1.661350345560872e-5
allele num: 120384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1349T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.487T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.695+12T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.135T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.443+12T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.100T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.533+12T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*310+12T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.132+12T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.622T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1124T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.536+12T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.579+12T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+12T>C
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14973
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

17-79872470-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872470
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872470
    reference: chr 17
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1347C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.485C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.132+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1122C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.133C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.98C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.695+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*310+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.579+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.443+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.533+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.536+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.620C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1715+10C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

17-79872485-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872485
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872485
    reference: chr 17
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1107A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.438A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.574A>G
  hgvsp: ENSP00000329466.6:p.Ile192Val
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1710A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.605A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.127A>G
  hgvsp: ENSP00000461044.1:p.Ile43Val
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.528A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.83A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.690A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1332A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*305A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.531A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.118A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.470A>G
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile192Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-79872497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872497
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872497
    reference: chr 17
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.593G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.71G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1095G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*293G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.426G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.106G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.519G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1698G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.562G>A
  hgvsp: ENSP00000329466.6:p.Gly188Arg
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.516G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.678G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1320G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.115G>A
  hgvsp: ENSP00000461044.1:p.Gly39Arg
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.458G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly188Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

17-79872498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872498
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872498
    reference: chr 17
allele count: 1
allele frequency: 8.312275568559649e-6
allele num: 120304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*292C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.677C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1319C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1697C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1094C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.70C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.561C>T
  hgvsp: ENST00000328666.6:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.457C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.425C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.114C>T
  hgvsp: ENST00000572902.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.592C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.518C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.105C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.515C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His187His
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

17-79872506-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872506
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872506
    reference: chr 17
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.97G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1311G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1689G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.417G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.510G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.106G>C
  hgvsp: ENSP00000461044.1:p.Glu36Gln
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.449G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1086G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.62G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*284G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.553G>C
  hgvsp: ENSP00000329466.6:p.Glu185Gln
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.669G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.584G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.507G>C
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu185Gln
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

17-79872507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872507
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872507
    reference: chr 17
allele count: 3
allele frequency: 2.494055833596595e-5
allele num: 120286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*283C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1310C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.552C>T
  hgvsp: ENST00000328666.6:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.583C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.509C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.105C>T
  hgvsp: ENST00000572902.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.96C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1085C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1688C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.668C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.416C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.506C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.448C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.61C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23427
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser184Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

17-79872510-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872510
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872510
    reference: chr 17
allele count: 1
allele frequency: 8.315316813570598e-6
allele num: 120260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.413C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.102C>G
  hgvsp: ENSP00000461044.1:p.Ile34Met
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.549C>G
  hgvsp: ENSP00000329466.6:p.Ile183Met
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.580C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.665C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.445C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.58C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1082C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1685C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.503C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*280C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1307C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.506C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.93C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile183Met
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-79872517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872517
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872517
    reference: chr 17
allele count: 79
allele frequency: 6.571176656518774e-4
allele num: 120222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.406C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1075C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.499C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.658C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.542C>T
  hgvsp: ENSP00000329466.6:p.Thr181Met
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1678C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.95C>T
  hgvsp: ENSP00000461044.1:p.Thr32Met
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.51C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1300C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.86C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.496C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.573C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.438C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23373
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Thr181Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

17-79872518-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872518
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872518
    reference: chr 17
allele count: 1
allele frequency: 8.318637074501714e-6
allele num: 120212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*272A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.498A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.94A>G
  hgvsp: ENSP00000461044.1:p.Thr32Ala
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1074A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1677A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.541A>G
  hgvsp: ENSP00000329466.6:p.Thr181Ala
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.572A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.85A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.50A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.657A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1299A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.405A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.437A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.495A>G
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr181Ala
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

17-79872520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872520
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872520
    reference: chr 17
allele count: 2
allele frequency: 1.664004259850905e-5
allele num: 120192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.48G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1675G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.83G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.570G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*270G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.435G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1072G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.539G>A
  hgvsp: ENSP00000329466.6:p.Arg180His
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.92G>A
  hgvsp: ENSP00000461044.1:p.Arg31His
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.496G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1297G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.493G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.403G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.655G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg180His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

17-79872521-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872521
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872521
    reference: chr 17
allele count: 3
allele frequency: 2.49617253544565e-5
allele num: 120184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.402C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.434C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.538C>T
  hgvsp: ENSP00000329466.6:p.Arg180Cys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1296C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.654C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*269C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.495C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.492C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.91C>T
  hgvsp: ENSP00000461044.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1071C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1674C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.82C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.569C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg180Cys
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

17-79872523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872523
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872523
    reference: chr 17
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.400C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*267C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1672C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.652C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1294C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.493C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.567C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.536C>T
  hgvsp: ENSP00000329466.6:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.89C>T
  hgvsp: ENSP00000461044.1:p.Pro30Leu
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.45C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1069C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.80C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.490C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.432C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro179Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

17-79872523-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872523
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872523
    reference: chr 17
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.89C>A
  hgvsp: ENSP00000461044.1:p.Pro30Gln
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.80C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.567C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.400C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1294C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.493C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.432C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1672C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.536C>A
  hgvsp: ENSP00000329466.6:p.Pro179Gln
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1069C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.652C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*267C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.490C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.45C>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro179Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

17-79872547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872547
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872547
    reference: chr 17
allele count: 1
allele frequency: 8.336112037345782e-6
allele num: 119960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.408G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1045G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.469G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.512G>A
  hgvsp: ENSP00000329466.6:p.Gly171Glu
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.628G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.56G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*243G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1648G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.466G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.543G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.65G>A
  hgvsp: ENSP00000461044.1:p.Gly22Glu
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1270G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.376G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.21G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly171Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-79872548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872548
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872548
    reference: chr 17
allele count: 1
allele frequency: 8.338197281747686e-6
allele num: 119930
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.511G>A
  hgvsp: ENSP00000329466.6:p.Gly171Arg
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.375G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.627G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*242G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.64G>A
  hgvsp: ENSP00000461044.1:p.Gly22Arg
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1647G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.55G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.465G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1044G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1269G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.407G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.468G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.542G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.20G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly171Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

17-79872549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872549
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872549
    reference: chr 17
allele count: 43
allele frequency: 3.585963039562346e-4
allele num: 119912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.374C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1646C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.541C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.464C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1043C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.510C>T
  hgvsp: ENST00000328666.6:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.626C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.467C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.54C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.63C>T
  hgvsp: ENST00000572902.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.19C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*241C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1268C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.406C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 9116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp170Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

17-79872555-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872555
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872555
    reference: chr 17
allele count: 1
allele frequency: 8.345155637152633e-6
allele num: 119830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.535C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.620C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.400C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.57C>G
  hgvsp: ENSP00000461044.1:p.Asn19Lys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.504C>G
  hgvsp: ENSP00000329466.6:p.Asn168Lys
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1262C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.368C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.48C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1037C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.458C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.13C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1640C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*235C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.461C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23226
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn168Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

17-79872564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872564
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872564
    reference: chr 17
allele count: 2
allele frequency: 1.671150921639733e-5
allele num: 119678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1253G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.495G>A
  hgvsp: ENST00000328666.6:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.452G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.39G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.4G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.611G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1631G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1028G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.449G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.48G>A
  hgvsp: ENST00000572902.1:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*226G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.359G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.526G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.391G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val165Val
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

17-79872565-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872565
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872565
    reference: chr 17
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*225T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.494T>C
  hgvsp: ENSP00000329466.6:p.Val165Ala
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000576156
  gene symbol: SIRT7
  hgvsc: ENST00000576156.1:n.3T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.47T>C
  hgvsp: ENSP00000461044.1:p.Val16Ala
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.451T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.610T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1027T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1630T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.358T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1252T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.38T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.525T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.390T>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.448T>C
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23113
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val165Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

17-79872580-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872580
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872580
    reference: chr 17
allele count: 1
allele frequency: 8.392359595823962e-6
allele num: 119156
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.23A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1237A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-2A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-2A>C
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.481-2A>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

17-79872589-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872589
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872589
    reference: chr 17
allele count: 7
allele frequency: 5.901893664738715e-5
allele num: 118606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.14C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1228C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-11C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-11C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

17-79872592-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872592
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872592
    reference: chr 17
allele count: 1
allele frequency: 8.442950980226608e-6
allele num: 118442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.11G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1225G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-14G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-14G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

17-79872593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872593
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872593
    reference: chr 17
allele count: 3
allele frequency: 2.536954977505666e-5
allele num: 118252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571233
  gene symbol: SIRT7
  hgvsc: ENST00000571233.1:n.10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1224C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-15C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-15C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

17-79872603-GGGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872603
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872600
    reference: chr 17
allele count: 1
allele frequency: 8.483922965979469e-6
allele num: 117870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-28_435-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-28_377-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-28_438-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1211_1213delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-28_481-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-28_512-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-28_1617-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-28_597-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-28_345-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-28_34-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-28_*212-26delTCC
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-28_1014-26delTCC
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: GGGA
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

17-79872605-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872605
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872605
    reference: chr 17
allele count: 1
allele frequency: 8.488676106074497e-6
allele num: 117804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1212C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-27C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-27C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20857
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

17-79872609-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872609
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872609
    reference: chr 17
allele count: 1
allele frequency: 8.504992430556738e-6
allele num: 117578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1208C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-31C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-31C>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-79872615-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872615
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872615
    reference: chr 17
allele count: 1
allele frequency: 8.530530769624486e-6
allele num: 117226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1202A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-37A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-37A>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17815
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

17-79872616-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872616
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872616
    reference: chr 17
allele count: 1
allele frequency: 8.543211564091173e-6
allele num: 117052
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1201C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-38C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-38C>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

17-79872617-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872617
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872617
    reference: chr 17
allele count: 1
allele frequency: 8.541606163623007e-6
allele num: 117074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1200G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-39G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-39G>C
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

17-79872621-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872621
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872621
    reference: chr 17
allele count: 1
allele frequency: 8.556662217202314e-6
allele num: 116868
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1196A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-43A>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-43A>C
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11487
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

17-79872628-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872628
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872628
    reference: chr 17
allele count: 4
allele frequency: 3.443585461182183e-5
allele num: 116158
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1189C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-50C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-50C>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12133
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-79872629-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79872629
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79872629
    reference: chr 17
allele count: 2
allele frequency: 1.721259273284335e-5
allele num: 116194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1014-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.481-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.438-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.435-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.597-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.345-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.1188C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.512-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.34-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*212-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.377-51C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1617-51C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10122
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

17-79873265-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873265
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873265
    reference: chr 17
allele count: 1
allele frequency: 1.349199924444804e-5
allele num: 74118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.552T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.552T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.603T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.440T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+51T>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+51T>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

17-79873266-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873266
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873266
    reference: chr 17
allele count: 1
allele frequency: 1.348690421600626e-5
allele num: 74146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.439C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.551C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.551C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.602C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+50C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+50C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19018
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

17-79873267-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873267
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873267
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 74212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.550C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.438C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.601C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.550C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+49C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+49C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19023
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

17-79873269-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873269
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873269
    reference: chr 17
allele count: 15
allele frequency: 2.022544630818187e-4
allele num: 74164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.548C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.548C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.599C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.436C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+47C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+47C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18386
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

17-79873274-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873274
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873274
    reference: chr 17
allele count: 49
allele frequency: 6.568716821277281e-4
allele num: 74596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.431C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.543C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.594C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+42C>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.543C>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19015
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18408
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-79873276-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873276
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873276
    reference: chr 17
allele count: 3
allele frequency: 3.996057223539441e-5
allele num: 75074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.429G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.541G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.541G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.592G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+40G>C
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+40G>C
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18308
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19047
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

17-79873281-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873281
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873281
    reference: chr 17
allele count: 1
allele frequency: 1.314993556531573e-5
allele num: 76046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.587G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.536G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.424G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+35G>A
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.536G>A
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17638
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

17-79873291-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873291
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873291
    reference: chr 17
allele count: 1
allele frequency: 1.247847463126108e-5
allele num: 80138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.526A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.526A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.577A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.414A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+25A>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+25A>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

17-79873292-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873292
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873292
    reference: chr 17
allele count: 1
allele frequency: 1.240233163834801e-5
allele num: 80630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.525C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.576C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.525C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.413C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+24C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+24C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

17-79873298-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873298
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873298
    reference: chr 17
allele count: 47
allele frequency: 5.536185450433471e-4
allele num: 84896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.407C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.519C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.519C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.570C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+18C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+18C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16532
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10195
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-79873306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873306
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873306
    reference: chr 17
allele count: 1
allele frequency: 1.089989536100453e-5
allele num: 91744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.562C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.511C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.511C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.399C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+10C>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+10C>T
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

17-79873306-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873306
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873306
    reference: chr 17
allele count: 2
allele frequency: 2.179979072200907e-5
allele num: 91744
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.562C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.399C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.511C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.511C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+10C>G
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+10C>G
  variant of: http://identifiers.org/hgnc/14935
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25823
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/17-79873311-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873311
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79873311
    reference: chr 17
allele count: 1
allele frequency: 1.048174080751331e-5
allele num: 95404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572671
  gene symbol: SIRT7
  hgvsc: ENST00000572671.1:n.557G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000573367
  gene symbol: SIRT7
  hgvsc: ENST00000573367.1:n.376+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000461044
  ensembl transcript: ENST00000572902
  gene symbol: SIRT7
  hgvsc: ENST00000572902.1:c.33+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000577065
  gene symbol: SIRT7
  hgvsc: ENST00000577065.1:n.437+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572350
  gene symbol: SIRT7
  hgvsc: ENST00000572350.1:n.344+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574495
  gene symbol: SIRT7
  hgvsc: ENST00000574495.2:n.511+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571915
  gene symbol: SIRT7
  hgvsc: ENST00000571915.1:n.434+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000571832
  gene symbol: SIRT7
  hgvsc: ENST00000571832.1:n.506G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000574992
  gene symbol: SIRT7
  hgvsc: ENST00000574992.1:n.1013+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000570367
  gene symbol: SIRT7
  hgvsc: ENST00000570367.1:n.506G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000572976
  gene symbol: SIRT7
  hgvsc: ENST00000572976.1:n.1616+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000329466
  ensembl transcript: ENST00000328666
  gene symbol: SIRT7
  hgvsc: ENST00000328666.6:c.480+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000575244
  gene symbol: SIRT7
  hgvsc: ENST00000575244.1:n.394G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000187531
  ensembl protein: ENSP00000459524
  ensembl transcript: ENST00000575360
  gene symbol: SIRT7
  hgvsc: ENST00000575360.1:c.*211+5G>T
  variant of: http://identifiers.org/hgnc/14935
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187531
  ensembl transcript: ENST00000536038
  gene symbol: SIRT7
  hgvsc: ENST00000536038.1:n.596+5G>T
  variant of: http://identifiers.org/hgnc/14935
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.480+5G>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

17-79873335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79873335
    reference: chr 17
allele count: 2
allele frequency: 1.854427445526194e-5
allele num: 107850
alternate allele: T
canonical: true
consequence: missense
filter: PASS
hgvs: p.Arg154His
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4406
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3728
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3754
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2901
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10056
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65858
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.83519e6

MQ
type: SiteQuality
SIO_000300: 5.917e1

VQSLOD
type: SiteQuality
SIO_000300: 8.45e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

MQRankSum
type: SiteQuality
SIO_000300: -1.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeDepth
all individuals: 35
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15108
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1412
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4407
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3728
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2902
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3751
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10058
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518141794443601e-5
allele num: 65870
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.065e0

QD
type: SiteQuality
SIO_000300: 1.413e1

FS
type: SiteQuality
SIO_000300: 3.783e0

VQSLOD
type: SiteQuality
SIO_000300: 8.100000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.758e0

DP
type: SiteQuality
SIO_000300: 1.835277e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeDepth
all individuals: 411
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6462
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31711
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2903
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517773123273533e-5
allele num: 65886
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.835228e6

QD
type: SiteQuality
SIO_000300: 1.416e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

FS
type: SiteQuality
SIO_000300: 4.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.499e0

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.932e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.32e-1

GenotypeDepth
all individuals: 6463
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15106
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4406
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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Latino
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allele frequency: 0.0e0
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African
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South Asian
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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QD
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

African
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allele frequency: 4.467754467754468e-3
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European (Non-Finnish)
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allele frequency: 3.035269835488375e-5
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European (Finnish)
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Latino
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Other
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East Asian
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FS
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
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allele count: 2
allele frequency: 3.035454103933948e-5
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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Other
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European (Finnish)
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ClippingRankSum
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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African
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Other
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South Asian
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Latino
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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DP
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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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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East Asian
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allele frequency: 1.392434439545138e-3
allele num: 8618
num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 1.945146858587823e-4
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

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

Other
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65820
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Latino
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East Asian
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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Latino
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QD
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

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

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

DP
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SIO_000300: 1.82732e6

ReadPosRankSum
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BaseQRankSum
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QD
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FS
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SIO_000300: 5.69e-1

MQRankSum
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InbreedingCoeff
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SIO_000300: -4.0e-4

VQSLOD
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MQ
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ClippingRankSum
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SIO_000300: -3.73e-1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.526904049349539e-5
allele num: 65492
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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SIO_000300: 1.71e0

MQ
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SIO_000300: 6.0e1

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

East Asian
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allele count: 2
allele frequency: 2.327205026762858e-4
allele num: 8594
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65378
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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SIO_000300: -8.32e-1

FS
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SIO_000300: 2.304e0

QD
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BaseQRankSum
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SIO_000300: -3.962e0

MQ
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SIO_000300: 5.958e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65342
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

East Asian
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allele 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

South Asian
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allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

InbreedingCoeff
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DP
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MQRankSum
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MQ
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SIO_000300: 5.969e1

ClippingRankSum
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BaseQRankSum
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SIO_000300: 3.57e0

ReadPosRankSum
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FS
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SIO_000300: 0.0e0

QD
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VQSLOD
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SIO_000300: 9.91e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.53888769197624e-5
allele num: 64982
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
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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BaseQRankSum
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DP
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MQ
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 1

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

East Asian
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allele frequency: 7.00770847932726e-4
allele num: 8562
num of homozygotes: 0

Other
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South Asian
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African
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European (Finnish)
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 64652
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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allele num: 64558
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Latino
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FS
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.656938838869916e-5
allele num: 64420
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

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

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

ReadPosRankSum
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SIO_000300: 1.05e0

ClippingRankSum
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SIO_000300: -2.7e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

QD
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SIO_000300: 1.404e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.36e-1

BaseQRankSum
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SIO_000300: -1.724e0

DP
type: SiteQuality
SIO_000300: 1.777531e6

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele 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
allele num: 64182
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

South Asian
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MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQ
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SIO_000300: 5.782e1

ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -2.327e0

QD
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 64134
num of homozygotes: 0

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

Other
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.74759e6

ReadPosRankSum
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SIO_000300: -1.08e0

ClippingRankSum
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MQ
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FS
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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SIO_000300: -1.264e0

InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

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

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

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

South Asian
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allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63982
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
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FS
type: SiteQuality
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DP
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SIO_000300: 1.727867e6

ClippingRankSum
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VQSLOD
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QD
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MQRankSum
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ReadPosRankSum
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SIO_000300: 8.58e-1

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567889620570712e-5
allele num: 63780
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

Latino
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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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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11422
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.570302440249992e-5
allele num: 63682
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6420
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South Asian
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allele num: 16376
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Other
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East Asian
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Latino
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European (Non-Finnish)
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1201
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11404
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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African
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East Asian
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allele frequency: 1.177856301531213e-4
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num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.334526335793241e-5
allele num: 63146
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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ReadPosRankSum
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MQ
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DP
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QD
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

Latino
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allele frequency: 8.837044892188053e-5
allele num: 11316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.58267915928083e-5
allele num: 63184
num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: -4.192e0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7000
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 39546
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 8.051529790660226e-5
allele num: 12420
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ClippingRankSum
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VQSLOD
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QD
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SIO_000300: 6.39e0

InbreedingCoeff
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SIO_000300: -8.800000000000001e-3

BaseQRankSum
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SIO_000300: 8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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DP
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SIO_000300: 8.72383e5

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

East Asian
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allele frequency: 1.846381093057607e-4
allele num: 5416
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12448
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.512562814070352e-5
allele num: 39800
num of homozygotes: 0

African
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allele count: 47
allele frequency: 7.376020087884494e-3
allele num: 6372
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5478
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2894
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.416029453412631e-4
allele num: 7062
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5516
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 7090
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40110
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2920
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 2.401921537229784e-4
allele num: 12490
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 0.0e0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.460024600246003e-5
allele num: 40650
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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DP
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SIO_000300: 9.22497e5

VQSLOD
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ClippingRankSum
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SIO_000300: -1.35e-1

MQRankSum
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FS
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 1
allele frequency: 7.776049766718506e-5
allele num: 12860
num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

Other
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QD
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SIO_000300: 1.784e1

MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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DP
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ClippingRankSum
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 43412
num of homozygotes: 0

Latino
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num of homozygotes: 0

African
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allele num: 6784
num of homozygotes: 0

South Asian
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East Asian
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Other
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European (Finnish)
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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FS
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MQRankSum
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QD
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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East Asian
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 46
allele frequency: 1.002004008016032e-3
allele num: 45908
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MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13632
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.39821029082774e-4
allele num: 7152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3786
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-2

DP
type: SiteQuality
SIO_000300: 1.171892e6

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 1.635e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.23e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.582e0

GenotypeDepth
all individuals: 5292
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 991
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2344
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 242
bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1656
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 2.668801708033093e-4
allele num: 7494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50062
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.283e1

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

FS
type: SiteQuality
SIO_000300: 1.635e0

DP
type: SiteQuality
SIO_000300: 1.171892e6

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.582e0

GenotypeDepth
all individuals: 22
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1578
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5928
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 242
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variant carriers: 0

GenotypeDepth
all individuals: 28088
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2701
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3258
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12378
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7442
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.205649228995533e-5
allele num: 13878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3976
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

QD
type: SiteQuality
SIO_000300: 4.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.074e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

FS
type: SiteQuality
SIO_000300: 9.622e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

DP
type: SiteQuality
SIO_000300: 1.213753e6

MQ
type: SiteQuality
SIO_000300: 6.0e1