16-84213030-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213030
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213030
    reference: chr 16
allele count: 142
allele frequency: 1.247518141725089e-3
allele num: 113826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1423C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2240C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.838C>T
  hgvsp: ENST00000568265.1:c.838C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1845C>T
  hgvsp: ENST00000341690.6:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3067C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2127C>T
  hgvsp: ENST00000567759.1:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2049C>T
  hgvsp: ENST00000566732.1:c.2049C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1848C>T
  hgvsp: ENST00000541676.1:c.1848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1131C>T
  hgvsp: ENST00000570117.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-139C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2127C>T
  hgvsp: ENST00000378541.4:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2072C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13294
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 34519
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Pro709Pro
num of homozygotes: 2
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

16-84213035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213035
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213035
    reference: chr 16
allele count: 1
allele frequency: 8.780710535096499e-6
allele num: 113886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2067G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1843G>A
  hgvsp: ENSP00000437900.1:p.Ala615Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-144G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1840G>A
  hgvsp: ENSP00000345305.6:p.Ala614Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2044G>A
  hgvsp: ENSP00000455933.1:p.Ala682Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2122G>A
  hgvsp: ENSP00000455265.1:p.Ala708Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.833G>A
  hgvsp: ENSP00000456101.1:p.Ala279Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2122G>A
  hgvsp: ENSP00000367802.4:p.Ala708Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1126G>A
  hgvsp: ENSP00000455247.1:p.Ala376Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1418G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3062G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2235G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala708Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/16-84213036-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213036
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213036
    reference: chr 16
allele count: 1
allele frequency: 8.779168788299123e-6
allele num: 113906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3061T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-145T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2234T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2121T>G
  hgvsp: ENST00000567759.1:c.2121T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1839T>G
  hgvsp: ENST00000341690.6:c.1839T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1125T>G
  hgvsp: ENST00000570117.1:c.1125T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2121T>G
  hgvsp: ENST00000378541.4:c.2121T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.832T>G
  hgvsp: ENST00000568265.1:c.832T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2043T>G
  hgvsp: ENST00000566732.1:c.2043T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1842T>G
  hgvsp: ENST00000541676.1:c.1842T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1417T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2066T>G
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro707Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-84213039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213039
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213039
    reference: chr 16
allele count: 3
allele frequency: 2.631071196786585e-5
allele num: 114022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1414C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2118C>T
  hgvsp: ENST00000567759.1:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2040C>T
  hgvsp: ENST00000566732.1:c.2040C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2231C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3058C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1836C>T
  hgvsp: ENST00000341690.6:c.1836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2118C>T
  hgvsp: ENST00000378541.4:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1122C>T
  hgvsp: ENST00000570117.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1839C>T
  hgvsp: ENST00000541676.1:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2063C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-148C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.829C>T
  hgvsp: ENST00000568265.1:c.829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro706Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-84213040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213040
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213040
    reference: chr 16
allele count: 1
allele frequency: 8.767776667192733e-6
allele num: 114054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1413C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1835C>T
  hgvsp: ENSP00000345305.6:p.Pro612Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2117C>T
  hgvsp: ENSP00000367802.4:p.Pro706Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2230C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1121C>T
  hgvsp: ENSP00000455247.1:p.Pro374Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2062C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2117C>T
  hgvsp: ENSP00000455265.1:p.Pro706Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1838C>T
  hgvsp: ENSP00000437900.1:p.Pro613Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3057C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.828C>T
  hgvsp: ENSP00000456101.1:p.Pro277Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2039C>T
  hgvsp: ENSP00000455933.1:p.Pro680Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-149C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro706Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

16-84213041-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213041
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213041
    reference: chr 16
allele count: 2
allele frequency: 1.753155680224404e-5
allele num: 114080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-150C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2116C>G
  hgvsp: ENSP00000455265.1:p.Pro706Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2038C>G
  hgvsp: ENSP00000455933.1:p.Pro680Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1120C>G
  hgvsp: ENSP00000455247.1:p.Pro374Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3056C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2061C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2116C>G
  hgvsp: ENSP00000367802.4:p.Pro706Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.827C>G
  hgvsp: ENSP00000456101.1:p.Pro277Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1834C>G
  hgvsp: ENSP00000345305.6:p.Pro612Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1837C>G
  hgvsp: ENSP00000437900.1:p.Pro613Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2229C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1412C>G
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro706Ala
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-84213045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213045
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213045
    reference: chr 16
allele count: 1
allele frequency: 8.76885303402315e-6
allele num: 114040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1408G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1833G>A
  hgvsp: ENST00000541676.1:c.1833G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2034G>A
  hgvsp: ENST00000566732.1:c.2034G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-154G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3052G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2112G>A
  hgvsp: ENST00000378541.4:c.2112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1116G>A
  hgvsp: ENST00000570117.1:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2112G>A
  hgvsp: ENST00000567759.1:c.2112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.823G>A
  hgvsp: ENST00000568265.1:c.823G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2057G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1830G>A
  hgvsp: ENST00000341690.6:c.1830G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2225G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu704Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

16-84213046-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213046
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213046
    reference: chr 16
allele count: 2
allele frequency: 1.753217153476629e-5
allele num: 114076
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2111A>G
  hgvsp: ENSP00000455265.1:p.Glu704Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-155A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1832A>G
  hgvsp: ENSP00000437900.1:p.Glu611Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1407A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2056A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2111A>G
  hgvsp: ENSP00000367802.4:p.Glu704Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1829A>G
  hgvsp: ENSP00000345305.6:p.Glu610Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.822A>G
  hgvsp: ENSP00000456101.1:p.Glu275Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1115A>G
  hgvsp: ENSP00000455247.1:p.Glu372Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2224A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2033A>G
  hgvsp: ENSP00000455933.1:p.Glu678Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3051A>G
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu704Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

16-84213047-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213047
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213047
    reference: chr 16
allele count: 2
allele frequency: 1.75404746452439e-5
allele num: 114022
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2110G>C
  hgvsp: ENSP00000455265.1:p.Glu704Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1828G>C
  hgvsp: ENSP00000345305.6:p.Glu610Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1406G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-156G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2032G>C
  hgvsp: ENSP00000455933.1:p.Glu678Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1831G>C
  hgvsp: ENSP00000437900.1:p.Glu611Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1114G>C
  hgvsp: ENSP00000455247.1:p.Glu372Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2110G>C
  hgvsp: ENSP00000367802.4:p.Glu704Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3050G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.821G>C
  hgvsp: ENSP00000456101.1:p.Glu275Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2055G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2223G>C
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu704Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

16-84213049-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213049
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213049
    reference: chr 16
allele count: 3
allele frequency: 2.631440450502605e-5
allele num: 114006
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2108C>T
  hgvsp: ENSP00000455265.1:p.Ala703Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2053C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2221C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2030C>T
  hgvsp: ENSP00000455933.1:p.Ala677Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3048C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1829C>T
  hgvsp: ENSP00000437900.1:p.Ala610Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1404C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.819C>T
  hgvsp: ENSP00000456101.1:p.Ala274Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1826C>T
  hgvsp: ENSP00000345305.6:p.Ala609Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2108C>T
  hgvsp: ENSP00000367802.4:p.Ala703Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1112C>T
  hgvsp: ENSP00000455247.1:p.Ala371Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-158C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala703Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

16-84213050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213050
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213050
    reference: chr 16
allele count: 11
allele frequency: 9.649461384609986e-5
allele num: 113996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1403G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2029G>A
  hgvsp: ENSP00000455933.1:p.Ala677Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2107G>A
  hgvsp: ENSP00000367802.4:p.Ala703Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-159G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2107G>A
  hgvsp: ENSP00000455265.1:p.Ala703Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3047G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.818G>A
  hgvsp: ENSP00000456101.1:p.Ala274Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1825G>A
  hgvsp: ENSP00000345305.6:p.Ala609Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1828G>A
  hgvsp: ENSP00000437900.1:p.Ala610Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2052G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2220G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1111G>A
  hgvsp: ENSP00000455247.1:p.Ala371Thr
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala703Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

16-84213051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213051
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213051
    reference: chr 16
allele count: 4
allele frequency: 3.508833488306812e-5
allele num: 113998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1402G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2051G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2106G>A
  hgvsp: ENST00000378541.4:c.2106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2219G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-160G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1827G>A
  hgvsp: ENST00000541676.1:c.1827G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.817G>A
  hgvsp: ENST00000568265.1:c.817G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1110G>A
  hgvsp: ENST00000570117.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2028G>A
  hgvsp: ENST00000566732.1:c.2028G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3046G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2106G>A
  hgvsp: ENST00000567759.1:c.2106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1824G>A
  hgvsp: ENST00000341690.6:c.1824G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13345
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala702Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

16-84213052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213052
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213052
    reference: chr 16
allele count: 4
allele frequency: 3.508402624285163e-5
allele num: 114012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-161C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1109C>T
  hgvsp: ENSP00000455247.1:p.Ala370Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1823C>T
  hgvsp: ENSP00000345305.6:p.Ala608Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1826C>T
  hgvsp: ENSP00000437900.1:p.Ala609Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2105C>T
  hgvsp: ENSP00000455265.1:p.Ala702Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2105C>T
  hgvsp: ENSP00000367802.4:p.Ala702Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2027C>T
  hgvsp: ENSP00000455933.1:p.Ala676Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1401C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2050C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2218C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.816C>T
  hgvsp: ENSP00000456101.1:p.Ala273Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3045C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala702Val
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: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

16-84213055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213055
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213055
    reference: chr 16
allele count: 1
allele frequency: 8.759328685049578e-6
allele num: 114164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1398C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2047C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1106C>T
  hgvsp: ENSP00000455247.1:p.Pro369Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3042C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.813C>T
  hgvsp: ENSP00000456101.1:p.Pro272Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2215C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2024C>T
  hgvsp: ENSP00000455933.1:p.Pro675Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2102C>T
  hgvsp: ENSP00000455265.1:p.Pro701Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1823C>T
  hgvsp: ENSP00000437900.1:p.Pro608Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2102C>T
  hgvsp: ENSP00000367802.4:p.Pro701Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-164C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1820C>T
  hgvsp: ENSP00000345305.6:p.Pro607Leu
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34374
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro701Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-84213062-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213062
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213062
    reference: chr 16
allele count: 1
allele frequency: 8.752122389679497e-6
allele num: 114258
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2095T>C
  hgvsp: ENSP00000455265.1:p.Ser699Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3035T>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2095T>C
  hgvsp: ENSP00000367802.4:p.Ser699Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1813T>C
  hgvsp: ENSP00000345305.6:p.Ser605Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2017T>C
  hgvsp: ENSP00000455933.1:p.Ser673Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1816T>C
  hgvsp: ENSP00000437900.1:p.Ser606Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1099T>C
  hgvsp: ENSP00000455247.1:p.Ser367Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1391T>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2208T>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-171T>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.806T>C
  hgvsp: ENSP00000456101.1:p.Ser270Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2040T>C
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser699Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-84213069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213069
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213069
    reference: chr 16
allele count: 1
allele frequency: 8.74018913769294e-6
allele num: 114414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2201C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1809C>T
  hgvsp: ENST00000541676.1:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2088C>T
  hgvsp: ENST00000378541.4:c.2088C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2010C>T
  hgvsp: ENST00000566732.1:c.2010C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1806C>T
  hgvsp: ENST00000341690.6:c.1806C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3028C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2088C>T
  hgvsp: ENST00000567759.1:c.2088C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1092C>T
  hgvsp: ENST00000570117.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1384C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-178C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2033C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.799C>T
  hgvsp: ENST00000568265.1:c.799C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp696Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

16-84213071-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213071
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213071
    reference: chr 16
allele count: 1
allele frequency: 8.740341922175995e-6
allele num: 114412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1090G>C
  hgvsp: ENSP00000455247.1:p.Asp364His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1804G>C
  hgvsp: ENSP00000345305.6:p.Asp602His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3026G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2008G>C
  hgvsp: ENSP00000455933.1:p.Asp670His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1382G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-180G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2086G>C
  hgvsp: ENSP00000367802.4:p.Asp696His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2086G>C
  hgvsp: ENSP00000455265.1:p.Asp696His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2199G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.797G>C
  hgvsp: ENSP00000456101.1:p.Asp267His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2031G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1807G>C
  hgvsp: ENSP00000437900.1:p.Asp603His
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp696His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

16-84213072-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213072
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213072
    reference: chr 16
allele count: 3
allele frequency: 2.621598475977419e-5
allele num: 114434
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.796A>C
  hgvsp: ENSP00000456101.1:p.Arg266Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-181A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2085A>C
  hgvsp: ENSP00000367802.4:p.Arg695Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1089A>C
  hgvsp: ENSP00000455247.1:p.Arg363Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1381A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2198A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3025A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2007A>C
  hgvsp: ENSP00000455933.1:p.Arg669Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2085A>C
  hgvsp: ENSP00000455265.1:p.Arg695Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2030A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1806A>C
  hgvsp: ENSP00000437900.1:p.Arg602Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1803A>C
  hgvsp: ENSP00000345305.6:p.Arg601Ser
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg695Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-84213075-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213075
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213075
    reference: chr 16
allele count: 2
allele frequency: 1.747640685075149e-5
allele num: 114440
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1800G>C
  hgvsp: ENSP00000345305.6:p.Gln600His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2082G>C
  hgvsp: ENSP00000455265.1:p.Gln694His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-184G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1803G>C
  hgvsp: ENSP00000437900.1:p.Gln601His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2027G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1378G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.793G>C
  hgvsp: ENSP00000456101.1:p.Gln265His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2082G>C
  hgvsp: ENSP00000367802.4:p.Gln694His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.2004G>C
  hgvsp: ENSP00000455933.1:p.Gln668His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1086G>C
  hgvsp: ENSP00000455247.1:p.Gln362His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3022G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2195G>C
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln694His
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

16-84213081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213081
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213081
    reference: chr 16
allele count: 1
allele frequency: 8.73591333973967e-6
allele num: 114470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1794G>A
  hgvsp: ENST00000341690.6:c.1794G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1372G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3016G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-190G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2076G>A
  hgvsp: ENST00000567759.1:c.2076G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2076G>A
  hgvsp: ENST00000378541.4:c.2076G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1998G>A
  hgvsp: ENST00000566732.1:c.1998G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1080G>A
  hgvsp: ENST00000570117.1:c.1080G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2021G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.787G>A
  hgvsp: ENST00000568265.1:c.787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2189G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1797G>A
  hgvsp: ENST00000541676.1:c.1797G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu692Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

16-84213091-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213091
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213091
    reference: chr 16
allele count: 1
allele frequency: 8.719916288803627e-6
allele num: 114680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2179G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3006G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2066G>A
  hgvsp: ENSP00000367802.4:p.Gly689Glu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1787G>A
  hgvsp: ENSP00000437900.1:p.Gly596Glu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1362G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1784G>A
  hgvsp: ENSP00000345305.6:p.Gly595Glu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-200G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2066G>A
  hgvsp: ENSP00000455265.1:p.Gly689Glu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1988G>A
  hgvsp: ENSP00000455933.1:p.Gly663Glu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.777G>A
  hgvsp: ENSP00000456101.1:p.Gly260Glu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1070G>A
  hgvsp: ENSP00000455247.1:p.Gly357Glu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2011G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly689Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-84213094-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213094
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213094
    reference: chr 16
allele count: 1
allele frequency: 8.724328662909389e-6
allele num: 114622
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3003G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1359G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1784G>A
  hgvsp: ENSP00000437900.1:p.Arg595Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1985G>A
  hgvsp: ENSP00000455933.1:p.Arg662Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2063G>A
  hgvsp: ENSP00000367802.4:p.Arg688Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2063G>A
  hgvsp: ENSP00000455265.1:p.Arg688Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1781G>A
  hgvsp: ENSP00000345305.6:p.Arg594Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-203G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2008G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.774G>A
  hgvsp: ENSP00000456101.1:p.Arg259Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1067G>A
  hgvsp: ENSP00000455247.1:p.Arg356Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2176G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg688Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-84213097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213097
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213097
    reference: chr 16
allele count: 2
allele frequency: 1.740098837613976e-5
allele num: 114936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2060C>T
  hgvsp: ENSP00000367802.4:p.Ala687Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1781C>T
  hgvsp: ENSP00000437900.1:p.Ala594Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2005C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-206C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1982C>T
  hgvsp: ENSP00000455933.1:p.Ala661Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.771C>T
  hgvsp: ENSP00000456101.1:p.Ala258Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1064C>T
  hgvsp: ENSP00000455247.1:p.Ala355Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2060C>T
  hgvsp: ENSP00000455265.1:p.Ala687Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2173C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1778C>T
  hgvsp: ENSP00000345305.6:p.Ala593Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.3000C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1356C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala687Val
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

16-84213097-GCCATGGCCTTGCGGAGCACA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213097
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213077
    reference: chr 16
allele count: 1
allele frequency: 8.700494188069882e-6
allele num: 114936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsp: ENSP00000455933.1:p.Val655ProfsTer32
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsp: ENSP00000456101.1:p.Val252ProfsTer32
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsp: ENSP00000345305.6:p.Val587ProfsTer32
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsp: ENSP00000455265.1:p.Val681ProfsTer32
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsp: ENSP00000455247.1:p.Val349ProfsTer32
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsp: ENSP00000437900.1:p.Val588ProfsTer32
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsp: ENSP00000367802.4:p.Val681ProfsTer32
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val681ProfsTer32
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: GCCATGGCCTTGCGGAGCACA
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-84213099-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213099
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213099
    reference: chr 16
allele count: 1
allele frequency: 8.696559641006019e-6
allele num: 114988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2171G>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1776G>T
  hgvsp: ENSP00000345305.6:p.Met592Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1980G>T
  hgvsp: ENSP00000455933.1:p.Met660Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1062G>T
  hgvsp: ENSP00000455247.1:p.Met354Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.769G>T
  hgvsp: ENSP00000456101.1:p.Met257Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.2003G>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1354G>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2058G>T
  hgvsp: ENSP00000367802.4:p.Met686Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2058G>T
  hgvsp: ENSP00000455265.1:p.Met686Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1779G>T
  hgvsp: ENSP00000437900.1:p.Met593Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2998G>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-208G>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met686Ile
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-84213109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213109
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213109
    reference: chr 16
allele count: 2
allele frequency: 1.734274466277033e-5
allele num: 115322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1993G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-218G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1766G>A
  hgvsp: ENSP00000345305.6:p.Arg589His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2048G>A
  hgvsp: ENSP00000455265.1:p.Arg683His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2988G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.759G>A
  hgvsp: ENSP00000456101.1:p.Arg254His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2048G>A
  hgvsp: ENSP00000367802.4:p.Arg683His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1970G>A
  hgvsp: ENSP00000455933.1:p.Arg657His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1052G>A
  hgvsp: ENSP00000455247.1:p.Arg351His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1769G>A
  hgvsp: ENSP00000437900.1:p.Arg590His
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1344G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2161G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13882
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg683His
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

16-84213110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213110
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213110
    reference: chr 16
allele count: 4
allele frequency: 3.463083529574734e-5
allele num: 115504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-219C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1768C>T
  hgvsp: ENSP00000437900.1:p.Arg590Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1992C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1969C>T
  hgvsp: ENSP00000455933.1:p.Arg657Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2047C>T
  hgvsp: ENSP00000455265.1:p.Arg683Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2987C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1051C>T
  hgvsp: ENSP00000455247.1:p.Arg351Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.758C>T
  hgvsp: ENSP00000456101.1:p.Arg254Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1765C>T
  hgvsp: ENSP00000345305.6:p.Arg589Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2047C>T
  hgvsp: ENSP00000367802.4:p.Arg683Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1343C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2160C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13956
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg683Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

16-84213111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213111
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213111
    reference: chr 16
allele count: 2
allele frequency: 1.731092146034933e-5
allele num: 115534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1968C>T
  hgvsp: ENST00000566732.1:c.1968C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2046C>T
  hgvsp: ENST00000378541.4:c.2046C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1764C>T
  hgvsp: ENST00000341690.6:c.1764C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1342C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2046C>T
  hgvsp: ENST00000567759.1:c.2046C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-220C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1050C>T
  hgvsp: ENST00000570117.1:c.1050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1767C>T
  hgvsp: ENST00000541676.1:c.1767C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2159C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1991C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.757C>T
  hgvsp: ENST00000568265.1:c.757C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2986C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu682Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS

16-84213113-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213113
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213113
    reference: chr 16
allele count: 2
allele frequency: 1.730582860307352e-5
allele num: 115568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.755C>T
  hgvsp: ENSP00000456101.1:p.Leu253Phe
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1340C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1762C>T
  hgvsp: ENSP00000345305.6:p.Leu588Phe
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2044C>T
  hgvsp: ENSP00000367802.4:p.Leu682Phe
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2044C>T
  hgvsp: ENSP00000455265.1:p.Leu682Phe
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1989C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2984C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1048C>T
  hgvsp: ENSP00000455247.1:p.Leu350Phe
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1765C>T
  hgvsp: ENSP00000437900.1:p.Leu589Phe
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-222C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2157C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1966C>T
  hgvsp: ENSP00000455933.1:p.Leu656Phe
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu682Phe
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

16-84213114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213114
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213114
    reference: chr 16
allele count: 40921
allele frequency: 3.511989563844213e-1
allele num: 116518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1988G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1965G>A
  hgvsp: ENST00000566732.1:c.1965G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1764G>A
  hgvsp: ENST00000541676.1:c.1764G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2043G>A
  hgvsp: ENST00000378541.4:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-223G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.754G>A
  hgvsp: ENST00000568265.1:c.754G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1761G>A
  hgvsp: ENST00000341690.6:c.1761G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2043G>A
  hgvsp: ENST00000567759.1:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1047G>A
  hgvsp: ENST00000570117.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2983G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1339G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2156G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16807
  bin: 2.25e1
  variant carriers: 2177
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 3.75e1
  variant carriers: 4409
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 1.25e1
  variant carriers: 1075
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.5e0
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 6.25e1
  variant carriers: 1559
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 7.5e0
  variant carriers: 489
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 3.25e1
  variant carriers: 3756
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 5.75e1
  variant carriers: 2204
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 1.75e1
  variant carriers: 1581
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 205
genotype depth: GenotypeDepth
  all individuals: 9779
  bin: 2.75e1
  variant carriers: 3097
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.75e1
  variant carriers: 973
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 592
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 5.25e1
  variant carriers: 3150
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 4.25e1
  variant carriers: 4330
genotype quality: GenotypeQuality
hgvs: p.Val681Val
num of homozygotes: 7452
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-84213117-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213117
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213117
    reference: chr 16
allele count: 69
allele frequency: 6.055074854765958e-4
allele num: 113954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-226T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2153T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2040T>G
  hgvsp: ENST00000567759.1:c.2040T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1044T>G
  hgvsp: ENST00000570117.1:c.1044T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1985T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1336T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1962T>G
  hgvsp: ENST00000566732.1:c.1962T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2040T>G
  hgvsp: ENST00000378541.4:c.2040T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2980T>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1758T>G
  hgvsp: ENST00000341690.6:c.1758T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1761T>G
  hgvsp: ENST00000541676.1:c.1761T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.751T>G
  hgvsp: ENST00000568265.1:c.751T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22728
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20835
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly680Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

16-84213121-A-AGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213121
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213124
    reference: chr 16
allele count: 1
allele frequency: 8.563990134283366e-6
allele num: 116768
alternate allele: AGCC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-233_*437-231dupGGC
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1754_1756dupGGC
  hgvsp: ENSP00000437900.1:p.Arg585dup
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1955_1957dupGGC
  hgvsp: ENSP00000455933.1:p.Arg652dup
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.744_746dupGGC
  hgvsp: ENSP00000456101.1:p.Arg249dup
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2033_2035dupGGC
  hgvsp: ENSP00000455265.1:p.Arg678dup
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2033_2035dupGGC
  hgvsp: ENSP00000367802.4:p.Arg678dup
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1978_1980dupGGC
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2146_2148dupGGC
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1751_1753dupGGC
  hgvsp: ENSP00000345305.6:p.Arg584dup
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1037_1039dupGGC
  hgvsp: ENSP00000455247.1:p.Arg346dup
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1329_*1331dupGGC
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2973_2975dupGGC
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg678dup
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

16-84213121-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213121
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213122
    reference: chr 16
allele count: 1
allele frequency: 8.563990134283366e-6
allele num: 116768
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1039_1040insA
  hgvsp: ENSP00000455247.1:p.Leu347HisfsTer41
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2148_2149insA
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2975_2976insA
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.746_747insA
  hgvsp: ENSP00000456101.1:p.Leu250HisfsTer41
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1980_1981insA
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2035_2036insA
  hgvsp: ENSP00000455265.1:p.Leu679HisfsTer41
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2035_2036insA
  hgvsp: ENSP00000367802.4:p.Leu679HisfsTer41
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1756_1757insA
  hgvsp: ENSP00000437900.1:p.Leu586HisfsTer41
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1957_1958insA
  hgvsp: ENSP00000455933.1:p.Leu653HisfsTer41
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1753_1754insA
  hgvsp: ENSP00000345305.6:p.Leu585HisfsTer41
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-231_*437-230insA
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1331_*1332insA
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23763
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu679HisfsTer41
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS

16-84213122-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213122
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213122
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 116774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.746C>G
  hgvsp: ENSP00000456101.1:p.Leu250Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1957C>G
  hgvsp: ENSP00000455933.1:p.Leu653Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1039C>G
  hgvsp: ENSP00000455247.1:p.Leu347Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-231C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2035C>G
  hgvsp: ENSP00000455265.1:p.Leu679Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1753C>G
  hgvsp: ENSP00000345305.6:p.Leu585Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2035C>G
  hgvsp: ENSP00000367802.4:p.Leu679Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1980C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1756C>G
  hgvsp: ENSP00000437900.1:p.Leu586Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1331C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2148C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2975C>G
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu679Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-84213123-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213123
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213123
    reference: chr 16
allele count: 1
allele frequency: 8.567071603584462e-6
allele num: 116726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2974G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1956G>C
  hgvsp: ENST00000566732.1:c.1956G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2034G>C
  hgvsp: ENST00000378541.4:c.2034G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1330G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1752G>C
  hgvsp: ENST00000341690.6:c.1752G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2034G>C
  hgvsp: ENST00000567759.1:c.2034G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1979G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1755G>C
  hgvsp: ENST00000541676.1:c.1755G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1038G>C
  hgvsp: ENST00000570117.1:c.1038G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-232G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2147G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.745G>C
  hgvsp: ENST00000568265.1:c.745G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg678Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

16-84213124-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213124
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213124
    reference: chr 16
allele count: 2
allele frequency: 1.712856702408277e-5
allele num: 116764
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2033G>A
  hgvsp: ENSP00000455265.1:p.Arg678Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2033G>A
  hgvsp: ENSP00000367802.4:p.Arg678Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1329G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2973G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2146G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1955G>A
  hgvsp: ENSP00000455933.1:p.Arg652Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1751G>A
  hgvsp: ENSP00000345305.6:p.Arg584Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.744G>A
  hgvsp: ENSP00000456101.1:p.Arg249Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-233G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1037G>A
  hgvsp: ENSP00000455247.1:p.Arg346Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1754G>A
  hgvsp: ENSP00000437900.1:p.Arg585Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1978G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg678Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-84213125-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213125
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213125
    reference: chr 16
allele count: 27
allele frequency: 2.311129371886395e-4
allele num: 116826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2145C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1328C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2032C>T
  hgvsp: ENSP00000367802.4:p.Arg678Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1753C>T
  hgvsp: ENSP00000437900.1:p.Arg585Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1954C>T
  hgvsp: ENSP00000455933.1:p.Arg652Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1036C>T
  hgvsp: ENSP00000455247.1:p.Arg346Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.743C>T
  hgvsp: ENSP00000456101.1:p.Arg249Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2972C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2032C>T
  hgvsp: ENSP00000455265.1:p.Arg678Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1750C>T
  hgvsp: ENSP00000345305.6:p.Arg584Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-234C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1977C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21557
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23818
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg678Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-84213125-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213125
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213125
    reference: chr 16
allele count: 64
allele frequency: 5.478232585212196e-4
allele num: 116826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1753C>A
  hgvsp: ENST00000541676.1:c.1753C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1750C>A
  hgvsp: ENST00000341690.6:c.1750C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2145C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.743C>A
  hgvsp: ENST00000568265.1:c.743C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2032C>A
  hgvsp: ENST00000378541.4:c.2032C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1328C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1954C>A
  hgvsp: ENST00000566732.1:c.1954C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-234C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1977C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2972C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2032C>A
  hgvsp: ENST00000567759.1:c.2032C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1036C>A
  hgvsp: ENST00000570117.1:c.1036C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 21557
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23818
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg678Arg
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

16-84213126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213126
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213126
    reference: chr 16
allele count: 1
allele frequency: 8.554466286848364e-6
allele num: 116898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1749G>A
  hgvsp: ENST00000341690.6:c.1749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1035G>A
  hgvsp: ENST00000570117.1:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2144G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2031G>A
  hgvsp: ENST00000378541.4:c.2031G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2031G>A
  hgvsp: ENST00000567759.1:c.2031G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1327G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2971G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-235G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1953G>A
  hgvsp: ENST00000566732.1:c.1953G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1976G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.742G>A
  hgvsp: ENST00000568265.1:c.742G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1752G>A
  hgvsp: ENST00000541676.1:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln677Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

16-84213140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213140
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213140
    reference: chr 16
allele count: 1
allele frequency: 8.542335816305611e-6
allele num: 117064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1021G>A
  hgvsp: ENSP00000455247.1:p.Glu341Lys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1735G>A
  hgvsp: ENSP00000345305.6:p.Glu579Lys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1939G>A
  hgvsp: ENSP00000455933.1:p.Glu647Lys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-249G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2017G>A
  hgvsp: ENSP00000455265.1:p.Glu673Lys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1962G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2957G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2130G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.728G>A
  hgvsp: ENSP00000456101.1:p.Glu244Lys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1738G>A
  hgvsp: ENSP00000437900.1:p.Glu580Lys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2017G>A
  hgvsp: ENSP00000367802.4:p.Glu673Lys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1313G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu673Lys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

16-84213141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213141
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213141
    reference: chr 16
allele count: 27
allele frequency: 2.305957911997814e-4
allele num: 117088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1734G>A
  hgvsp: ENST00000341690.6:c.1734G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.727G>A
  hgvsp: ENST00000568265.1:c.727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1312G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2956G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1737G>A
  hgvsp: ENST00000541676.1:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1938G>A
  hgvsp: ENST00000566732.1:c.1938G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2016G>A
  hgvsp: ENST00000567759.1:c.2016G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-250G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2016G>A
  hgvsp: ENST00000378541.4:c.2016G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1020G>A
  hgvsp: ENST00000570117.1:c.1020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1961G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2129G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24086
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22377
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Glu672Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

16-84213144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213144
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213144
    reference: chr 16
allele count: 2
allele frequency: 1.707271268331825e-5
allele num: 117146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1017G>A
  hgvsp: ENST00000570117.1:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2126G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-253G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2013G>A
  hgvsp: ENST00000567759.1:c.2013G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1935G>A
  hgvsp: ENST00000566732.1:c.1935G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2013G>A
  hgvsp: ENST00000378541.4:c.2013G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1309G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1731G>A
  hgvsp: ENST00000341690.6:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1734G>A
  hgvsp: ENST00000541676.1:c.1734G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.724G>A
  hgvsp: ENST00000568265.1:c.724G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1958G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2953G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24205
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg671Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

16-84213146-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213146
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213146
    reference: chr 16
allele count: 1
allele frequency: 8.535336292249914e-6
allele num: 117160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.722A>C
  hgvsp: ENST00000568265.1:c.722A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1015A>C
  hgvsp: ENST00000570117.1:c.1015A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1956A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1933A>C
  hgvsp: ENST00000566732.1:c.1933A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2124A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1729A>C
  hgvsp: ENST00000341690.6:c.1729A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1307A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2011A>C
  hgvsp: ENST00000378541.4:c.2011A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2011A>C
  hgvsp: ENST00000567759.1:c.2011A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2951A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-255A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1732A>C
  hgvsp: ENST00000541676.1:c.1732A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg671Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

16-84213148-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213148
    reference: chr 16
allele count: 1
allele frequency: 8.535190590805893e-6
allele num: 117162
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1730G>C
  hgvsp: ENSP00000437900.1:p.Arg577Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1013G>C
  hgvsp: ENSP00000455247.1:p.Arg338Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1954G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-257G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2009G>C
  hgvsp: ENSP00000367802.4:p.Arg670Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2009G>C
  hgvsp: ENSP00000455265.1:p.Arg670Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1727G>C
  hgvsp: ENSP00000345305.6:p.Arg576Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2949G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1305G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2122G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1931G>C
  hgvsp: ENSP00000455933.1:p.Arg644Pro
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.720G>C
  hgvsp: ENSP00000456101.1:p.Arg241Pro
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg670Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

16-84213148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213148
    reference: chr 16
allele count: 2
allele frequency: 1.707038118161179e-5
allele num: 117162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1013G>A
  hgvsp: ENSP00000455247.1:p.Arg338Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1727G>A
  hgvsp: ENSP00000345305.6:p.Arg576Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1305G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2949G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2009G>A
  hgvsp: ENSP00000367802.4:p.Arg670Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-257G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2009G>A
  hgvsp: ENSP00000455265.1:p.Arg670Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1931G>A
  hgvsp: ENSP00000455933.1:p.Arg644Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1954G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1730G>A
  hgvsp: ENSP00000437900.1:p.Arg577Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.720G>A
  hgvsp: ENSP00000456101.1:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2122G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg670Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

16-84213149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213149
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213149
    reference: chr 16
allele count: 2
allele frequency: 1.70712554201236e-5
allele num: 117156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1729C>T
  hgvsp: ENSP00000437900.1:p.Arg577Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1930C>T
  hgvsp: ENSP00000455933.1:p.Arg644Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1726C>T
  hgvsp: ENSP00000345305.6:p.Arg576Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.2008C>T
  hgvsp: ENSP00000455265.1:p.Arg670Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1012C>T
  hgvsp: ENSP00000455247.1:p.Arg338Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.719C>T
  hgvsp: ENSP00000456101.1:p.Arg241Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-258C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.2008C>T
  hgvsp: ENSP00000367802.4:p.Arg670Trp
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1304C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2948C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1953C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2121C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg670Trp
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-84213158-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213158
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213158
    reference: chr 16
allele count: 3
allele frequency: 2.557675584428871e-5
allele num: 117294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2112A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1921A>G
  hgvsp: ENSP00000455933.1:p.Thr641Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1003A>G
  hgvsp: ENSP00000455247.1:p.Thr335Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1944A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1720A>G
  hgvsp: ENSP00000437900.1:p.Thr574Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1999A>G
  hgvsp: ENSP00000367802.4:p.Thr667Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2939A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.710A>G
  hgvsp: ENSP00000456101.1:p.Thr238Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-267A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1717A>G
  hgvsp: ENSP00000345305.6:p.Thr573Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1295A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1999A>G
  hgvsp: ENSP00000455265.1:p.Thr667Ala
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24422
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr667Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-84213161-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213161
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213161
    reference: chr 16
allele count: 6
allele frequency: 5.114217524718718e-5
allele num: 117320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2109A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1292A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-270A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1996A>G
  hgvsp: ENSP00000367802.4:p.Ser666Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.1000A>G
  hgvsp: ENSP00000455247.1:p.Ser334Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1714A>G
  hgvsp: ENSP00000345305.6:p.Ser572Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1996A>G
  hgvsp: ENSP00000455265.1:p.Ser666Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1941A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1918A>G
  hgvsp: ENSP00000455933.1:p.Ser640Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1717A>G
  hgvsp: ENSP00000437900.1:p.Ser573Gly
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2936A>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.707A>G
  hgvsp: ENSP00000456101.1:p.Ser237Gly
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser666Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-84213163-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213163
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213163
    reference: chr 16
allele count: 1
allele frequency: 8.524713143402724e-6
allele num: 117306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2107G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1916G>C
  hgvsp: ENSP00000455933.1:p.Gly639Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1290G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.705G>C
  hgvsp: ENSP00000456101.1:p.Gly236Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1715G>C
  hgvsp: ENSP00000437900.1:p.Gly572Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.998G>C
  hgvsp: ENSP00000455247.1:p.Gly333Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2934G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1712G>C
  hgvsp: ENSP00000345305.6:p.Gly571Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1939G>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1994G>C
  hgvsp: ENSP00000367802.4:p.Gly665Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1994G>C
  hgvsp: ENSP00000455265.1:p.Gly665Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-272G>C
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly665Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-84213174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213174
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213174
    reference: chr 16
allele count: 1
allele frequency: 8.526893823118114e-6
allele num: 117276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1701C>T
  hgvsp: ENST00000341690.6:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1983C>T
  hgvsp: ENST00000378541.4:c.1983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1704C>T
  hgvsp: ENST00000541676.1:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2923C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1983C>T
  hgvsp: ENST00000567759.1:c.1983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-283C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1928C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1905C>T
  hgvsp: ENST00000566732.1:c.1905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1279C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.694C>T
  hgvsp: ENST00000568265.1:c.694C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2096C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.987C>T
  hgvsp: ENST00000570117.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22836
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg661Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

16-84213175-CGGTGGGTGAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213175
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213165
    reference: chr 16
allele count: 1
allele frequency: 8.530239699735563e-6
allele num: 117230
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsp: ENSP00000455265.1:p.Phe658AlafsTer53
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsp: ENSP00000455933.1:p.Phe632AlafsTer53
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsp: ENSP00000437900.1:p.Phe565AlafsTer53
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsp: ENSP00000455247.1:p.Phe326AlafsTer53
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsp: ENSP00000456101.1:p.Phe229AlafsTer53
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsp: ENSP00000367802.4:p.Phe658AlafsTer53
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsp: ENSP00000345305.6:p.Phe564AlafsTer53
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe658AlafsTer53
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: CGGTGGGTGAA
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

16-84213176-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213176
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213176
    reference: chr 16
allele count: 13
allele frequency: 1.110048500580641e-4
allele num: 117112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.692C>T
  hgvsp: ENSP00000456101.1:p.Arg232Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1981C>T
  hgvsp: ENSP00000367802.4:p.Arg661Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1981C>T
  hgvsp: ENSP00000455265.1:p.Arg661Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2094C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.985C>T
  hgvsp: ENSP00000455247.1:p.Arg329Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1699C>T
  hgvsp: ENSP00000345305.6:p.Arg567Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2921C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1702C>T
  hgvsp: ENSP00000437900.1:p.Arg568Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-285C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1277C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1903C>T
  hgvsp: ENSP00000455933.1:p.Arg635Cys
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1926C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22514
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24651
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg661Cys
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-84213180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213180
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213180
    reference: chr 16
allele count: 1
allele frequency: 8.534316486592589e-6
allele num: 117174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1698C>T
  hgvsp: ENST00000541676.1:c.1698C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.981C>T
  hgvsp: ENST00000570117.1:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1922C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1899C>T
  hgvsp: ENST00000566732.1:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.688C>T
  hgvsp: ENST00000568265.1:c.688C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1977C>T
  hgvsp: ENST00000378541.4:c.1977C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1695C>T
  hgvsp: ENST00000341690.6:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-289C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2090C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1273C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2917C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1977C>T
  hgvsp: ENST00000567759.1:c.1977C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr659Thr
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: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

16-84213181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213181
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213181
    reference: chr 16
allele count: 2
allele frequency: 1.706542885422711e-5
allele num: 117196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1921C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1976C>T
  hgvsp: ENSP00000367802.4:p.Thr659Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1898C>T
  hgvsp: ENSP00000455933.1:p.Thr633Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2916C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1694C>T
  hgvsp: ENSP00000345305.6:p.Thr565Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1976C>T
  hgvsp: ENSP00000455265.1:p.Thr659Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1697C>T
  hgvsp: ENSP00000437900.1:p.Thr566Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2089C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.687C>T
  hgvsp: ENSP00000456101.1:p.Thr230Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1272C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.980C>T
  hgvsp: ENSP00000455247.1:p.Thr327Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-290C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24605
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22862
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr659Ile
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

16-84213181-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213181
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213181
    reference: chr 16
allele count: 1
allele frequency: 8.532714427113554e-6
allele num: 117196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1976C>A
  hgvsp: ENSP00000367802.4:p.Thr659Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1272C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1921C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2916C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1694C>A
  hgvsp: ENSP00000345305.6:p.Thr565Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.687C>A
  hgvsp: ENSP00000456101.1:p.Thr230Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1898C>A
  hgvsp: ENSP00000455933.1:p.Thr633Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-290C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2089C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1976C>A
  hgvsp: ENSP00000455265.1:p.Thr659Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.980C>A
  hgvsp: ENSP00000455247.1:p.Thr327Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1697C>A
  hgvsp: ENSP00000437900.1:p.Thr566Asn
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr659Asn
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

16-84213183-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213183
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213183
    reference: chr 16
allele count: 7
allele frequency: 5.972798170617246e-5
allele num: 117198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.978C>T
  hgvsp: ENST00000570117.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1692C>T
  hgvsp: ENST00000341690.6:c.1692C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1974C>T
  hgvsp: ENST00000378541.4:c.1974C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.685C>T
  hgvsp: ENST00000568265.1:c.685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-292C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1695C>T
  hgvsp: ENST00000541676.1:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1896C>T
  hgvsp: ENST00000566732.1:c.1896C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1974C>T
  hgvsp: ENST00000567759.1:c.1974C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1919C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1270C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2914C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2087C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Phe658Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-84213187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213187
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213187
    reference: chr 16
allele count: 13
allele frequency: 1.109290736569049e-4
allele num: 117192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1266C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-296C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1688C>T
  hgvsp: ENSP00000345305.6:p.Thr563Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.974C>T
  hgvsp: ENSP00000455247.1:p.Thr325Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1970C>T
  hgvsp: ENSP00000367802.4:p.Thr657Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.681C>T
  hgvsp: ENSP00000456101.1:p.Thr228Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1892C>T
  hgvsp: ENSP00000455933.1:p.Thr631Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2083C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1915C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1970C>T
  hgvsp: ENSP00000455265.1:p.Thr657Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1691C>T
  hgvsp: ENSP00000437900.1:p.Thr564Ile
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2910C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24606
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr657Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-84213187-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213187
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213187
    reference: chr 16
allele count: 1
allele frequency: 8.533005665915763e-6
allele num: 117192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2910C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-296C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1688C>A
  hgvsp: ENSP00000345305.6:p.Thr563Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1970C>A
  hgvsp: ENSP00000367802.4:p.Thr657Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.681C>A
  hgvsp: ENSP00000456101.1:p.Thr228Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1970C>A
  hgvsp: ENSP00000455265.1:p.Thr657Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1915C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1691C>A
  hgvsp: ENSP00000437900.1:p.Thr564Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.974C>A
  hgvsp: ENSP00000455247.1:p.Thr325Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1266C>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1892C>A
  hgvsp: ENSP00000455933.1:p.Thr631Asn
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2083C>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr657Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

16-84213193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213193
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213193
    reference: chr 16
allele count: 4
allele frequency: 3.417167851284855e-5
allele num: 117056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1685C>T
  hgvsp: ENSP00000437900.1:p.Ala562Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1682C>T
  hgvsp: ENSP00000345305.6:p.Ala561Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2077C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1964C>T
  hgvsp: ENSP00000455265.1:p.Ala655Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-302C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1909C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2904C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.675C>T
  hgvsp: ENSP00000456101.1:p.Ala226Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.968C>T
  hgvsp: ENSP00000455247.1:p.Ala323Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1886C>T
  hgvsp: ENSP00000455933.1:p.Ala629Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1964C>T
  hgvsp: ENSP00000367802.4:p.Ala655Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1260C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6821
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24594
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala655Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

16-84213194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213194
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213194
    reference: chr 16
allele count: 1
allele frequency: 8.543357539513029e-6
allele num: 117050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1684G>A
  hgvsp: ENSP00000437900.1:p.Ala562Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1908G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1259G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.674G>A
  hgvsp: ENSP00000456101.1:p.Ala226Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-303G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1963G>A
  hgvsp: ENSP00000455265.1:p.Ala655Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1963G>A
  hgvsp: ENSP00000367802.4:p.Ala655Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1885G>A
  hgvsp: ENSP00000455933.1:p.Ala629Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.967G>A
  hgvsp: ENSP00000455247.1:p.Ala323Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2903G>A
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1681G>A
  hgvsp: ENSP00000345305.6:p.Ala561Thr
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2076G>A
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala655Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

16-84213195-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213195
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213195
    reference: chr 16
allele count: 4
allele frequency: 3.417927027257968e-5
allele num: 117030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1680A>C
  hgvsp: ENST00000341690.6:c.1680A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1962A>C
  hgvsp: ENST00000567759.1:c.1962A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1907A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1258A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.966A>C
  hgvsp: ENST00000570117.1:c.966A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2902A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1962A>C
  hgvsp: ENST00000378541.4:c.1962A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1884A>C
  hgvsp: ENST00000566732.1:c.1884A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1683A>C
  hgvsp: ENST00000541676.1:c.1683A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2075A>C
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.673A>C
  hgvsp: ENST00000568265.1:c.673A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-304A>C
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr654Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

16-84213196-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213196
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213196
    reference: chr 16
allele count: 1
allele frequency: 8.550662676357418e-6
allele num: 116950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.965C>G
  hgvsp: ENSP00000455247.1:p.Thr322Arg
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.672C>G
  hgvsp: ENSP00000456101.1:p.Thr225Arg
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1961C>G
  hgvsp: ENSP00000455265.1:p.Thr654Arg
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1883C>G
  hgvsp: ENSP00000455933.1:p.Thr628Arg
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2901C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-305C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2074C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1961C>G
  hgvsp: ENSP00000367802.4:p.Thr654Arg
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1257C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1679C>G
  hgvsp: ENSP00000345305.6:p.Thr560Arg
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1682C>G
  hgvsp: ENSP00000437900.1:p.Thr561Arg
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1906C>G
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr654Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

16-84213205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213205
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213205
    reference: chr 16
allele count: 1
allele frequency: 8.568833439015613e-6
allele num: 116702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1874C>T
  hgvsp: ENSP00000455933.1:p.Pro625Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1952C>T
  hgvsp: ENSP00000367802.4:p.Pro651Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1673C>T
  hgvsp: ENSP00000437900.1:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2892C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.956C>T
  hgvsp: ENSP00000455247.1:p.Pro319Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2065C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1670C>T
  hgvsp: ENSP00000345305.6:p.Pro557Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1897C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1952C>T
  hgvsp: ENSP00000455265.1:p.Pro651Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.663C>T
  hgvsp: ENSP00000456101.1:p.Pro222Leu
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-314C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1248C>T
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro651Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

16-84213206-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213206
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213206
    reference: chr 16
allele count: 1
allele frequency: 8.568833439015613e-6
allele num: 116702
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1951C>G
  hgvsp: ENSP00000455265.1:p.Pro651Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1669C>G
  hgvsp: ENSP00000345305.6:p.Pro557Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1247C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.662C>G
  hgvsp: ENSP00000456101.1:p.Pro222Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2891C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.955C>G
  hgvsp: ENSP00000455247.1:p.Pro319Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1896C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2064C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1873C>G
  hgvsp: ENSP00000455933.1:p.Pro625Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-315C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1951C>G
  hgvsp: ENSP00000367802.4:p.Pro651Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1672C>G
  hgvsp: ENSP00000437900.1:p.Pro558Ala
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro651Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

16-84213209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213209
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213209
    reference: chr 16
allele count: 2
allele frequency: 1.714648239913582e-5
allele num: 116642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-318C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1893C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1244C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.659C>T
  hgvsp: ENSP00000456101.1:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1669C>T
  hgvsp: ENSP00000437900.1:p.Pro557Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1666C>T
  hgvsp: ENSP00000345305.6:p.Pro556Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2888C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.952C>T
  hgvsp: ENSP00000455247.1:p.Pro318Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1948C>T
  hgvsp: ENSP00000367802.4:p.Pro650Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1948C>T
  hgvsp: ENSP00000455265.1:p.Pro650Ser
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2061C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1870C>T
  hgvsp: ENSP00000455933.1:p.Pro624Ser
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro650Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-84213209-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213209
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213209
    reference: chr 16
allele count: 5
allele frequency: 4.286620599783954e-5
allele num: 116642
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.659C>G
  hgvsp: ENSP00000456101.1:p.Pro221Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1948C>G
  hgvsp: ENSP00000367802.4:p.Pro650Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1870C>G
  hgvsp: ENSP00000455933.1:p.Pro624Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1666C>G
  hgvsp: ENSP00000345305.6:p.Pro556Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1893C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1948C>G
  hgvsp: ENSP00000455265.1:p.Pro650Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2061C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1669C>G
  hgvsp: ENSP00000437900.1:p.Pro557Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-318C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.952C>G
  hgvsp: ENSP00000455247.1:p.Pro318Ala
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2888C>G
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1244C>G
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro650Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

16-84213211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84213211
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84213211
    reference: chr 16
allele count: 99
allele frequency: 8.493188291410727e-4
allele num: 116564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456133
  ensembl transcript: ENST00000566903
  gene symbol: TAF1C
  hgvsc: ENST00000566903.1:c.*437-320C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000345305
  ensembl transcript: ENST00000341690
  gene symbol: TAF1C
  hgvsc: ENST00000341690.6:c.1664C>T
  hgvsp: ENSP00000345305.6:p.Ala555Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000544090
  gene symbol: TAF1C
  hgvsc: ENST00000544090.1:n.1891C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000456101
  ensembl transcript: ENST00000568265
  gene symbol: TAF1C
  hgvsc: ENST00000568265.1:c.657C>T
  hgvsp: ENSP00000456101.1:p.Ala220Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455933
  ensembl transcript: ENST00000566732
  gene symbol: TAF1C
  hgvsc: ENST00000566732.1:c.1868C>T
  hgvsp: ENSP00000455933.1:p.Ala623Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564208
  gene symbol: TAF1C
  hgvsc: ENST00000564208.1:n.2059C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455247
  ensembl transcript: ENST00000570117
  gene symbol: TAF1C
  hgvsc: ENST00000570117.1:c.950C>T
  hgvsp: ENSP00000455247.1:p.Ala317Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000367802
  ensembl transcript: ENST00000378541
  gene symbol: TAF1C
  hgvsc: ENST00000378541.4:c.1946C>T
  hgvsp: ENSP00000367802.4:p.Ala649Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455265
  ensembl transcript: ENST00000567759
  gene symbol: TAF1C
  hgvsc: ENST00000567759.1:c.1946C>T
  hgvsp: ENSP00000455265.1:p.Ala649Val
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000455787
  ensembl transcript: ENST00000563428
  gene symbol: TAF1C
  hgvsc: ENST00000563428.1:c.*1242C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103168
  ensembl transcript: ENST00000564774
  gene symbol: TAF1C
  hgvsc: ENST00000564774.1:n.2886C>T
  variant of: http://identifiers.org/hgnc/11534
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103168
  ensembl protein: ENSP00000437900
  ensembl transcript: ENST00000541676
  gene symbol: TAF1C
  hgvsc: ENST00000541676.1:c.1667C>T
  hgvsp: ENSP00000437900.1:p.Ala556Val
  variant of: http://identifiers.org/hgnc/11534
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24069
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
hgvs: p.Ala649Val
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 10
bin: 7.25e1
variant carriers: 8

GenotypeDepth
all individuals: 15
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 259
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1965
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 963
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5835
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 9.75e1
variant carriers: 138

GenotypeQuality
all individuals: 203
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3693
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 563
bin: 3.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 311
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 922
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39179
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.191895113230036e-4
allele num: 8390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

African
type: Population
allele count: 136
allele frequency: 1.523297491039427e-2
allele num: 8928
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.995394652680057e-5
allele num: 62536
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

DP
type: SiteQuality
SIO_000300: 1.358952e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 1.758e0

QD
type: SiteQuality
SIO_000300: 1.173e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

GenotypeDepth
all individuals: 2743
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 627
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 569
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 935
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39695
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5868
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.372673973999491e-5
allele num: 15692
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.451e0

MQRankSum
type: SiteQuality
SIO_000300: 7.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

QD
type: SiteQuality
SIO_000300: 1.495e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.044e0

VQSLOD
type: SiteQuality
SIO_000300: -1.627e-1

DP
type: SiteQuality
SIO_000300: 1.356531e6

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2768
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 810
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3873
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8962
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6068
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.365372374283896e-5
allele num: 15710
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.357137e6

VQSLOD
type: SiteQuality
SIO_000300: -4.197e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.017e1

FS
type: SiteQuality
SIO_000300: 2.548e0

QD
type: SiteQuality
SIO_000300: 1.793e1

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeDepth
all individuals: 34489
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 295
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.381519409383186e-4
allele num: 8398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.791981712678038e-5
allele num: 11374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15718
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.894e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 1.4256e1

DP
type: SiteQuality
SIO_000300: 1.35621e6

QD
type: SiteQuality
SIO_000300: 1.232e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

GenotypeDepth
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5860
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 777
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39761
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3910
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596016343207354e-5
allele num: 62656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.085000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

DP
type: SiteQuality
SIO_000300: 1.356605e6

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 778
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5860
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.191727043503239e-5
allele num: 62662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.23e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 2.288e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

DP
type: SiteQuality
SIO_000300: 1.35618e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2747
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3966
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5838
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.384880602732728e-5
allele num: 15662
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.925e0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

FS
type: SiteQuality
SIO_000300: 7.153e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.534e0

DP
type: SiteQuality
SIO_000300: 1.355535e6

QD
type: SiteQuality
SIO_000300: 1.718e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.675e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.274859765425803e-4
allele num: 15688
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.36e-1

DP
type: SiteQuality
SIO_000300: 1.355381e6

ClippingRankSum
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SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.217e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1012
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
all individuals: 3949
bin: 2.25e1
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GenotypeQuality
all individuals: 39427
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GenotypeQuality
all individuals: 1980
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variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1017
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15662
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.107419712070875e-4
allele num: 9030
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596474983237013e-5
allele num: 62638
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.277e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 3.331e0

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

InbreedingCoeff
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SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 1.355476e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

GenotypeDepth
all individuals: 13
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13334
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variant carriers: 1

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1007
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GenotypeQuality
all individuals: 5848
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 211
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GenotypeQuality
all individuals: 2002
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 8.25e1
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GenotypeQuality
all individuals: 451
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 236
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.31858407079646e-4
allele num: 9040
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.469e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.121e0

DP
type: SiteQuality
SIO_000300: 1.354665e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.016e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 459
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variant carriers: 11

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 247
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1975
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GenotypeQuality
all individuals: 328
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GenotypeQuality
all individuals: 641
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 39367
bin: 6.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5835
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.638986629134412e-4
allele num: 11368
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.526077637532746e-4
allele num: 8398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62616
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.232e0

DP
type: SiteQuality
SIO_000300: 1.35586e6

FS
type: SiteQuality
SIO_000300: 1.726e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1974
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.798169980644026e-5
allele num: 11366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.193357815743254e-5
allele num: 62630
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.395497569710924e-5
allele num: 15636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.669e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-2

DP
type: SiteQuality
SIO_000300: 1.35555e6

QD
type: SiteQuality
SIO_000300: 1.324e1

MQRankSum
type: SiteQuality
SIO_000300: 7.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1975
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variant carriers: 0

GenotypeQuality
all individuals: 422
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.39877143588431e-5
allele num: 15628
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.208480565371025e-4
allele num: 9056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596627921829097e-5
allele num: 62632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

BaseQRankSum
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SIO_000300: -1.297e0

FS
type: SiteQuality
SIO_000300: 3.219e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
type: SiteQuality
SIO_000300: 1.355812e6

QD
type: SiteQuality
SIO_000300: 1.27e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.036e0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.594743724683443e-5
allele num: 62706
num of homozygotes: 0

Other
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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9078
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.899e1

MQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ClippingRankSum
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DP
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QD
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FS
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.2e-1

ReadPosRankSum
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SIO_000300: 1.42e0

InbreedingCoeff
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SIO_000300: 5.0e-4

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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Latino
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allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.379992344009187e-5
allele num: 15674
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62750
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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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: 6110
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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MQ
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MQRankSum
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SIO_000300: 1.86e-1

ClippingRankSum
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DP
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FS
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 1.96e0

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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bin: 1.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 15676
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.591849729385546e-5
allele num: 62820
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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QD
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MQRankSum
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ClippingRankSum
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SIO_000300: -1.28e-1

DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6114
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.591596371160274e-5
allele num: 62830
num of homozygotes: 0

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

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

Other
type: Population
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BaseQRankSum
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SIO_000300: -2.268e0

QD
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ClippingRankSum
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SIO_000300: 2.53e-1

MQ
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FS
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: -4.17e-1

MQRankSum
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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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variant carriers: 3

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.262997607135088e-4
allele num: 9194
num of homozygotes: 0

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

Other
type: Population
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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

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

East Asian
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FS
type: SiteQuality
SIO_000300: 1.174e0

VQSLOD
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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European (Finnish)
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 62848
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Latino
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num of homozygotes: 0

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

Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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ReadPosRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 1975
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GenotypeQuality
all individuals: 3852
bin: 2.25e1
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GenotypeQuality
all individuals: 193
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.587856076725206e-5
allele num: 62978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6128
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.28e-1

MQ
type: SiteQuality
SIO_000300: 5.866e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.549e0

FS
type: SiteQuality
SIO_000300: 2.258e0

MQRankSum
type: SiteQuality
SIO_000300: -1.08e0

DP
type: SiteQuality
SIO_000300: 1.359378e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.683e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.004e1

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
all individuals: 38283
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 839
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variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.390593047034765e-5
allele num: 15648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.239e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.361485e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.626e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

GenotypeDepth
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
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variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 436
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GenotypeQuality
all individuals: 477
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38997
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GenotypeQuality
all individuals: 2001
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GenotypeQuality
all individuals: 1235
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variant carriers: 0

GenotypeQuality
all individuals: 486
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variant carriers: 2

GenotypeQuality
all individuals: 421
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.171381453761258e-5
allele num: 63064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 6.99e0

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.365034e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

FS
type: SiteQuality
SIO_000300: 2.766e0

GenotypeQuality
all individuals: 2068
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5944
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 486
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3768
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.585690726880629e-5
allele num: 63064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15744
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

QD
type: SiteQuality
SIO_000300: 6.99e0

FS
type: SiteQuality
SIO_000300: 2.766e0

MQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

DP
type: SiteQuality
SIO_000300: 1.365034e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
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variant carriers: 0

GenotypeQuality
all individuals: 495
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variant carriers: 0

GenotypeQuality
all individuals: 440
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GenotypeQuality
all individuals: 1172
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
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variant carriers: 0

GenotypeQuality
all individuals: 3667
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 61
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5961
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GenotypeQuality
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GenotypeQuality
all individuals: 492
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GenotypeQuality
all individuals: 504
bin: 4.75e1
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GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
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variant carriers: 1

GenotypeQuality
all individuals: 2085
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584987003106575e-5
allele num: 63092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

DP
type: SiteQuality
SIO_000300: 1.366814e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.291e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

MQ
type: SiteQuality
SIO_000300: 5.9e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.653e0

VQSLOD
type: SiteQuality
SIO_000300: -8.93e-2

QD
type: SiteQuality
SIO_000300: 1.153e1

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 6077
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 457
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63190
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.183431952662722e-4
allele num: 8450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.626016260162602e-4
allele num: 6150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15888
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.212e0

FS
type: SiteQuality
SIO_000300: 4.156e0

DP
type: SiteQuality
SIO_000300: 1.377452e6

QD
type: SiteQuality
SIO_000300: 1.253e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 223
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1327
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2159
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GenotypeQuality
all individuals: 995
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3309
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6160
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 778
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GenotypeQuality
all individuals: 373
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variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.773469029654326e-5
allele num: 11398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.254705144291092e-4
allele num: 15940
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.187648456057007e-3
allele num: 842
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.835000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.766e0

QD
type: SiteQuality
SIO_000300: 3.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: -1.696e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.380494e6

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.25e1
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GenotypeQuality
all individuals: 2170
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39094
bin: 6.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6187
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 4.75e1
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GenotypeQuality
all individuals: 210
bin: 1.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 874
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 515
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15950
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.365184484389782e-4
allele num: 8456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6158
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-1

DP
type: SiteQuality
SIO_000300: 1.381526e6

VQSLOD
type: SiteQuality
SIO_000300: -3.439e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

QD
type: SiteQuality
SIO_000300: 1.736e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 3.955e0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
all individuals: 68
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variant carriers: 1

GenotypeDepth
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 779
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
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variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6154
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15966
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.122691572914456e-4
allele num: 9422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.384394e6

FS
type: SiteQuality
SIO_000300: 1.553e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.617e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

MQRankSum
type: SiteQuality
SIO_000300: -1.164e0

QD
type: SiteQuality
SIO_000300: 1.57e1

VQSLOD
type: SiteQuality
SIO_000300: -4.078e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

GenotypeDepth
all individuals: 62
bin: 9.25e1
variant carriers: 62

GenotypeDepth
all individuals: 149
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variant carriers: 149

GenotypeDepth
all individuals: 3869
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variant carriers: 3815

GenotypeQuality
all individuals: 342
bin: 4.25e1
variant carriers: 116

GenotypeQuality
all individuals: 219
bin: 1.75e1
variant carriers: 83

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 376

GenotypeQuality
all individuals: 762
bin: 7.25e1
variant carriers: 216

GenotypeQuality
all individuals: 516
bin: 8.25e1
variant carriers: 393

GenotypeQuality
all individuals: 297
bin: 2.5e0
variant carriers: 32

GenotypeQuality
all individuals: 152
bin: 1.25e1
variant carriers: 61

GenotypeQuality
all individuals: 511
bin: 3.75e1
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GenotypeQuality
all individuals: 635
bin: 7.75e1
variant carriers: 298

GenotypeQuality
all individuals: 1733
bin: 2.25e1
variant carriers: 108

GenotypeQuality
all individuals: 568
bin: 2.75e1
variant carriers: 90

GenotypeQuality
all individuals: 311
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variant carriers: 46

GenotypeQuality
all individuals: 629
bin: 3.25e1
variant carriers: 129

GenotypeQuality
all individuals: 30735
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variant carriers: 30695

GenotypeQuality
all individuals: 2363
bin: 6.75e1
variant carriers: 267

GenotypeQuality
all individuals: 472
bin: 4.75e1
variant carriers: 159

GenotypeQuality
all individuals: 599
bin: 5.25e1
variant carriers: 231

GenotypeQuality
all individuals: 463
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variant carriers: 194

GenotypeQuality
all individuals: 18583
bin: 6.25e1
variant carriers: 209

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 302

European (Non-Finnish)
type: Population
allele count: 23323
allele frequency: 3.647866616616617e-1
allele num: 63936
num of homozygotes: 4231

Latino
type: Population
allele count: 5818
allele frequency: 5.12238070082761e-1
allele num: 11358
num of homozygotes: 1478

European (Finnish)
type: Population
allele count: 2271
allele frequency: 3.666451404585082e-1
allele num: 6194
num of homozygotes: 381

African
type: Population
allele count: 1667
allele frequency: 1.739720308912544e-1
allele num: 9582
num of homozygotes: 132

South Asian
type: Population
allele count: 4427
allele frequency: 2.742874845105329e-1
allele num: 16140
num of homozygotes: 614

East Asian
type: Population
allele count: 3116
allele frequency: 3.692818203365726e-1
allele num: 8438
num of homozygotes: 559

Other
type: Population
allele count: 299
allele frequency: 3.436781609195402e-1
allele num: 870
num of homozygotes: 57

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-2

FS
type: SiteQuality
SIO_000300: 2.463e0

QD
type: SiteQuality
SIO_000300: 1.69e1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.775e0

DP
type: SiteQuality
SIO_000300: 1.982353e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

GenotypeDepth
all individuals: 309
bin: 4.75e1
variant carriers: 12

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 56
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 963
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 577
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 36685
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1060
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1859
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 591
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 975
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 2125
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variant carriers: 3

GenotypeQuality
all individuals: 848
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variant carriers: 6

GenotypeQuality
all individuals: 2438
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variant carriers: 9

GenotypeQuality
all individuals: 352
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variant carriers: 8

GenotypeQuality
all individuals: 629
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
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variant carriers: 6

GenotypeQuality
all individuals: 286
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variant carriers: 1

GenotypeQuality
all individuals: 870
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 7054
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 661
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 888
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1004
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 17
allele frequency: 3.088662790697674e-3
allele num: 5504
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.688097306689834e-4
allele num: 9208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 6.079610904902086e-4
allele num: 62504
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.76273576590869e-4
allele num: 11346
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.191183754333828e-5
allele num: 16152
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.373042240151875e-4
allele num: 8428
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.231527093596059e-3
allele num: 812
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.510701e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 5.1e-1

FS
type: SiteQuality
SIO_000300: 1.87374e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.638e2

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.251e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.536e0

GenotypeDepth
all individuals: 1992
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 39288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
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variant carriers: 0

GenotypeQuality
all individuals: 664
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variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 747
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variant carriers: 0

GenotypeQuality
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 543
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variant carriers: 1

GenotypeQuality
all individuals: 421
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variant carriers: 0

GenotypeQuality
all individuals: 2235
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GenotypeQuality
all individuals: 7571
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variant carriers: 0

GenotypeQuality
all individuals: 753
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variant carriers: 0

GenotypeQuality
all individuals: 2596
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variant carriers: 0

GenotypeQuality
all individuals: 184
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 408
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variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
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variant carriers: 0

GenotypeQuality
all individuals: 290
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variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.164468006411046e-5
allele num: 16222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.95e-1

FS
type: SiteQuality
SIO_000300: 9.815e0

MQ
type: SiteQuality
SIO_000300: 5.753e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

QD
type: SiteQuality
SIO_000300: 1.64e1

VQSLOD
type: SiteQuality
SIO_000300: 6.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

DP
type: SiteQuality
SIO_000300: 1.494279e6

GenotypeDepth
all individuals: 1359
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 4.25e1
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GenotypeQuality
all individuals: 7571
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GenotypeQuality
all individuals: 39288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
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variant carriers: 0

GenotypeQuality
all individuals: 184
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variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 887
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variant carriers: 0

GenotypeQuality
all individuals: 408
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variant carriers: 0

GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 2596
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GenotypeQuality
all individuals: 753
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variant carriers: 0

GenotypeQuality
all individuals: 747
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GenotypeQuality
all individuals: 898
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GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 2235
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GenotypeQuality
all individuals: 664
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GenotypeQuality
all individuals: 153
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GenotypeQuality
all individuals: 290
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variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561670362619858e-5
allele num: 64034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.64e1

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

DP
type: SiteQuality
SIO_000300: 1.494279e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.753e1

FS
type: SiteQuality
SIO_000300: 9.815e0

GenotypeDepth
all individuals: 7133
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 889
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GenotypeQuality
all individuals: 654
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variant carriers: 0

GenotypeQuality
all individuals: 2599
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 542
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variant carriers: 1

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 7.75e1
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GenotypeQuality
all individuals: 7548
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 8.25e1
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GenotypeQuality
all individuals: 537
bin: 5.25e1
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GenotypeQuality
all individuals: 426
bin: 4.25e1
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GenotypeQuality
all individuals: 401
bin: 7.5e0
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GenotypeQuality
all individuals: 748
bin: 2.75e1
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GenotypeQuality
all individuals: 2234
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GenotypeQuality
all individuals: 289
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GenotypeQuality
all individuals: 336
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GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 39305
bin: 6.25e1
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GenotypeQuality
all individuals: 744
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.494642e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.031e1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2220
bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.758101243650377e-5
allele num: 11418
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6098
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64030
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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

VQSLOD
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SIO_000300: -3.231e0

InbreedingCoeff
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SIO_000300: 9.0e-4

FS
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DP
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 1.67e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.22e0

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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.124218945263684e-5
allele num: 64016
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

QD
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SIO_000300: 2.069e1

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

FS
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SIO_000300: 3.214e0

DP
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SIO_000300: 1.495999e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
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SIO_000300: -3.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.889e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.23e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 26

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7517
bin: 6.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.590384014985951e-4
allele num: 64060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.077274615704196e-4
allele num: 9628
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.230466346745417e-4
allele num: 16254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.499219e6

BaseQRankSum
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SIO_000300: 5.5e-1

MQRankSum
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SIO_000300: -3.0e-2

VQSLOD
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SIO_000300: 4.76e0

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

QD
type: SiteQuality
SIO_000300: 1.379e1

GenotypeDepth
all individuals: 30
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variant carriers: 3

GenotypeDepth
all individuals: 4
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variant carriers: 2

GenotypeDepth
all individuals: 63
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 64

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

South Asian
type: Population
allele count: 1
allele frequency: 6.152331733727083e-5
allele num: 16254
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.162790697674419e-3
allele num: 860
num of homozygotes: 0

African
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allele count: 62
allele frequency: 6.439551308683008e-3
allele num: 9628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64060
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

MQRankSum
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SIO_000300: -3.0e-2

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.379e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 690
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GenotypeQuality
all individuals: 311
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.147037128104254e-5
allele num: 16268
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64096
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

BaseQRankSum
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MQ
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SIO_000300: 5.913e1

MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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FS
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SIO_000300: 1.143e0

DP
type: SiteQuality
SIO_000300: 1.49778e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.78e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 525
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64166
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QD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.729e0

DP
type: SiteQuality
SIO_000300: 1.504295e6

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
all individuals: 506
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GenotypeQuality
all individuals: 200
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

East Asian
type: Population
allele count: 24
allele frequency: 2.811621368322399e-3
allele num: 8536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.064835845550279e-4
allele num: 9686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64180
num of homozygotes: 0

Other
type: Population
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BaseQRankSum
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SIO_000300: -1.433e0

ClippingRankSum
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SIO_000300: -1.9e-1

QD
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SIO_000300: 1.307e1

ReadPosRankSum
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SIO_000300: 3.03e-1

MQ
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SIO_000300: 5.951e1

InbreedingCoeff
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SIO_000300: -9.0e-4

DP
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SIO_000300: 1.505233e6

FS
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SIO_000300: 5.21e-1

MQRankSum
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SIO_000300: 2.24e-1

VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.114294612270321e-5
allele num: 64220
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

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

South Asian
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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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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQRankSum
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: 5.77e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.557098813490704e-5
allele num: 64222
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -7.0e-4

ClippingRankSum
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MQRankSum
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MQ
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SIO_000300: 5.95e1

FS
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BaseQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6024
num of homozygotes: 0

South Asian
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allele frequency: 6.093102607847916e-5
allele num: 16412
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.962e1

ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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QD
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MQRankSum
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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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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: 9708
num of homozygotes: 0

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

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

Other
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.11448860097172e-5
allele num: 64216
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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allele num: 64210
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Other
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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DP
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QD
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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QD
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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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: 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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South Asian
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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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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64336
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

DP
type: SiteQuality
SIO_000300: 1.511138e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

QD
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SIO_000300: 1.276e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64326
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.755034144633164e-5
allele num: 11422
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

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

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

MQRankSum
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SIO_000300: 5.45e-1

VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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FS
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SIO_000300: 5.895e0

QD
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SIO_000300: 2.68e0

BaseQRankSum
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MQ
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SIO_000300: 5.893e1

ReadPosRankSum
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SIO_000300: 1.04e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64334
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.026483268322726e-4
allele num: 9742
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11414
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

FS
type: SiteQuality
SIO_000300: 2.226e0

ClippingRankSum
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SIO_000300: -1.105e0

VQSLOD
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SIO_000300: 4.85e-1

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 9.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

QD
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SIO_000300: 8.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.801e0

DP
type: SiteQuality
SIO_000300: 1.509939e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.555064846204087e-5
allele num: 64306
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.510338e6

QD
type: SiteQuality
SIO_000300: 2.81e0

VQSLOD
type: SiteQuality
SIO_000300: -4.786e-1

ClippingRankSum
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SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 4.743e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.244903675578102e-4
allele num: 64262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.688618709895306e-4
allele num: 5922
num of homozygotes: 0

African
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allele count: 4
allele frequency: 4.1211621677313e-4
allele num: 9706
num of homozygotes: 1

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

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

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

FS
type: SiteQuality
SIO_000300: 3.221e0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.172058134083451e-4
allele num: 8532
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64278
num of homozygotes: 0

Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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SIO_000300: 1.506879e6

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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South Asian
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num of homozygotes: 0

African
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.110710175132983e-5
allele num: 64294
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele num: 8532
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Other
type: Population
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Latino
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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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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 2.3e-3

MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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SIO_000300: -9.379999999999999e-1

VQSLOD
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FS
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SIO_000300: 2.686e0

DP
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SIO_000300: 1.506672e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64292
num of homozygotes: 0

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

African
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allele count: 7
allele frequency: 7.195723684210526e-4
allele num: 9728
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.3e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Non-Finnish)
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allele count: 13
allele frequency: 2.021772939346812e-4
allele num: 64300
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 2.2e-3

MQ
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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DP
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SIO_000300: 1.506724e6

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64300
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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allele num: 8530
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.167e1

InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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FS
type: SiteQuality
SIO_000300: 5.25e-1

VQSLOD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

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

African
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allele count: 0
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num of homozygotes: 0

Other
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East Asian
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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: 4
allele frequency: 6.225680933852139e-5
allele num: 64250
num of homozygotes: 0

QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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African
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allele frequency: 1.030715316429602e-4
allele num: 9702
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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African
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European (Non-Finnish)
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East Asian
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allele num: 8518
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Latino
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South Asian
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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FS
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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East Asian
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Other
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European (Non-Finnish)
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African
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South Asian
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BaseQRankSum
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SIO_000300: 6.14e-1

FS
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

South Asian
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allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

African
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allele count: 1
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allele num: 9642
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e-1

DP
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SIO_000300: 1.490894e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

South Asian
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allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.12217053295451e-5
allele num: 64058
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QD
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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 frequency: 3.12217053295451e-5
allele num: 64058
num of homozygotes: 0

Other
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Latino
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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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ClippingRankSum
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QD
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FS
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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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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