4-107163635-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163635
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163635
    reference: chr 4
allele count: 1
allele frequency: 8.436255652291287e-6
allele num: 118536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.973C>A
  hgvsp: ENSP00000355338.4:p.Leu325Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1045C>A
  hgvsp: ENSP00000378196.3:p.Leu349Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.378C>A
  hgvsp: ENSP00000422160.1:p.Leu127Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.815C>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1162C>A
  hgvsp: ENSP00000405847.2:p.Leu388Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1162C>A
  hgvsp: ENSP00000378198.2:p.Leu388Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1162C>A
  hgvsp: ENSP00000273980.4:p.Leu388Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*801C>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12680
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu388Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

4-107163639-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163639
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163639
    reference: chr 4
allele count: 2
allele frequency: 1.6839836316791e-5
allele num: 118766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1041C>T
  hgvsp: ENST00000394706.3:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.811C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1158C>T
  hgvsp: ENST00000432496.2:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.969C>T
  hgvsp: ENST00000361687.4:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*797C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1158C>T
  hgvsp: ENST00000273980.5:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.374C>T
  hgvsp: ENST00000508666.1:c.374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1158C>T
  hgvsp: ENST00000394708.2:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys386Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-107163641-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163641
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163641
    reference: chr 4
allele count: 1
allele frequency: 8.40745909771149e-6
allele num: 118942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.809T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.372T>G
  hgvsp: ENSP00000422160.1:p.Cys125Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*795T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1039T>G
  hgvsp: ENSP00000378196.3:p.Cys347Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1156T>G
  hgvsp: ENSP00000273980.4:p.Cys386Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1156T>G
  hgvsp: ENSP00000405847.2:p.Cys386Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1156T>G
  hgvsp: ENSP00000378198.2:p.Cys386Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.967T>G
  hgvsp: ENSP00000355338.4:p.Cys323Gly
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys386Gly
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-107163641-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163641
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163641
    reference: chr 4
allele count: 2
allele frequency: 1.681491819542298e-5
allele num: 118942
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1156T>C
  hgvsp: ENSP00000273980.4:p.Cys386Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.809T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.372T>C
  hgvsp: ENSP00000422160.1:p.Cys125Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1039T>C
  hgvsp: ENSP00000378196.3:p.Cys347Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1156T>C
  hgvsp: ENSP00000405847.2:p.Cys386Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*795T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.967T>C
  hgvsp: ENSP00000355338.4:p.Cys323Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1156T>C
  hgvsp: ENSP00000378198.2:p.Cys386Arg
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys386Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-107163645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163645
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163645
    reference: chr 4
allele count: 2
allele frequency: 1.67838740538091e-5
allele num: 119162
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1152G>A
  hgvsp: ENST00000273980.5:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1152G>A
  hgvsp: ENST00000394708.2:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1152G>A
  hgvsp: ENST00000432496.2:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.368G>A
  hgvsp: ENST00000508666.1:c.368G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.963G>A
  hgvsp: ENST00000361687.4:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*791G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1035G>A
  hgvsp: ENST00000394706.3:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.805G>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser384Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

4-107163647-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163647
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163647
    reference: chr 4
allele count: 2
allele frequency: 1.676867611302088e-5
allele num: 119270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.803T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1033T>C
  hgvsp: ENSP00000378196.3:p.Ser345Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1150T>C
  hgvsp: ENSP00000378198.2:p.Ser384Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1150T>C
  hgvsp: ENSP00000405847.2:p.Ser384Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.366T>C
  hgvsp: ENSP00000422160.1:p.Ser123Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1150T>C
  hgvsp: ENSP00000273980.4:p.Ser384Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*789T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.961T>C
  hgvsp: ENSP00000355338.4:p.Ser321Pro
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser384Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

4-107163651-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163651
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163651
    reference: chr 4
allele count: 3
allele frequency: 2.512142019762184e-5
allele num: 119420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.799A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.362A>G
  hgvsp: ENST00000508666.1:c.362A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1146A>G
  hgvsp: ENST00000394708.2:c.1146A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1029A>G
  hgvsp: ENST00000394706.3:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*785A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.957A>G
  hgvsp: ENST00000361687.4:c.957A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1146A>G
  hgvsp: ENST00000432496.2:c.1146A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1146A>G
  hgvsp: ENST00000273980.5:c.1146A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4054
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr382Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

4-107163651-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163651
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163651
    reference: chr 4
allele count: 1
allele frequency: 8.373806732540612e-6
allele num: 119420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1146A>C
  hgvsp: ENST00000394708.2:c.1146A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1146A>C
  hgvsp: ENST00000432496.2:c.1146A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*785A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.957A>C
  hgvsp: ENST00000361687.4:c.957A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.799A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1029A>C
  hgvsp: ENST00000394706.3:c.1029A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1146A>C
  hgvsp: ENST00000273980.5:c.1146A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.362A>C
  hgvsp: ENST00000508666.1:c.362A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr382Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-107163652-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163652
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163652
    reference: chr 4
allele count: 1
allele frequency: 8.373946976167747e-6
allele num: 119418
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1145C>T
  hgvsp: ENSP00000273980.4:p.Thr382Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1028C>T
  hgvsp: ENSP00000378196.3:p.Thr343Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1145C>T
  hgvsp: ENSP00000405847.2:p.Thr382Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1145C>T
  hgvsp: ENSP00000378198.2:p.Thr382Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.956C>T
  hgvsp: ENSP00000355338.4:p.Thr319Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.798C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.361C>T
  hgvsp: ENSP00000422160.1:p.Thr121Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*784C>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4052
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr382Ile
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

4-107163662-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163662
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163662
    reference: chr 4
allele count: 1
allele frequency: 8.360085607276618e-6
allele num: 119616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1135A>G
  hgvsp: ENSP00000378198.2:p.Thr379Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*774A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.946A>G
  hgvsp: ENSP00000355338.4:p.Thr316Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1018A>G
  hgvsp: ENSP00000378196.3:p.Thr340Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.351A>G
  hgvsp: ENSP00000422160.1:p.Thr118Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1135A>G
  hgvsp: ENSP00000273980.4:p.Thr379Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.788A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1135A>G
  hgvsp: ENSP00000405847.2:p.Thr379Ala
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4070
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr379Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

4-107163664-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163664
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163664
    reference: chr 4
allele count: 1
allele frequency: 8.36050497450046e-6
allele num: 119610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1133A>T
  hgvsp: ENSP00000378198.2:p.Asp378Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1133A>T
  hgvsp: ENSP00000405847.2:p.Asp378Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1016A>T
  hgvsp: ENSP00000378196.3:p.Asp339Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.349A>T
  hgvsp: ENSP00000422160.1:p.Asp117Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.786A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*772A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1133A>T
  hgvsp: ENSP00000273980.4:p.Asp378Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.944A>T
  hgvsp: ENSP00000355338.4:p.Asp315Val
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4077
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51511
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp378Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

4-107163667-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163667
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163667
    reference: chr 4
allele count: 256
allele frequency: 2.140826225121258e-3
allele num: 119580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.941A>T
  hgvsp: ENSP00000355338.4:p.Asp314Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*769A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1130A>T
  hgvsp: ENSP00000273980.4:p.Asp377Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1013A>T
  hgvsp: ENSP00000378196.3:p.Asp338Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1130A>T
  hgvsp: ENSP00000378198.2:p.Asp377Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.783A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.346A>T
  hgvsp: ENSP00000422160.1:p.Asp116Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1130A>T
  hgvsp: ENSP00000405847.2:p.Asp377Val
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 39886
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13337
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp377Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-107163667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163667
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163667
    reference: chr 4
allele count: 1
allele frequency: 8.362602441879913e-6
allele num: 119580
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1130A>G
  hgvsp: ENSP00000273980.4:p.Asp377Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1130A>G
  hgvsp: ENSP00000378198.2:p.Asp377Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1013A>G
  hgvsp: ENSP00000378196.3:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1130A>G
  hgvsp: ENSP00000405847.2:p.Asp377Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*769A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.783A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.346A>G
  hgvsp: ENSP00000422160.1:p.Asp116Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.941A>G
  hgvsp: ENSP00000355338.4:p.Asp314Gly
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13337
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp377Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-107163675-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163675
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163675
    reference: chr 4
allele count: 18
allele frequency: 1.506276150627615e-4
allele num: 119500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1122G>T
  hgvsp: ENST00000394708.2:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.933G>T
  hgvsp: ENST00000361687.4:c.933G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1122G>T
  hgvsp: ENST00000432496.2:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.338G>T
  hgvsp: ENST00000508666.1:c.338G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*761G>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1122G>T
  hgvsp: ENST00000273980.5:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1005G>T
  hgvsp: ENST00000394706.3:c.1005G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.775G>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser374Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP

4-107163675-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163675
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163675
    reference: chr 4
allele count: 2
allele frequency: 1.673640167364017e-5
allele num: 119500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1122G>C
  hgvsp: ENST00000394708.2:c.1122G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1122G>C
  hgvsp: ENST00000273980.5:c.1122G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*761G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1122G>C
  hgvsp: ENST00000432496.2:c.1122G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.338G>C
  hgvsp: ENST00000508666.1:c.338G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.775G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.933G>C
  hgvsp: ENST00000361687.4:c.933G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1005G>C
  hgvsp: ENST00000394706.3:c.1005G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 51418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser374Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

4-107163675-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163675
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163675
    reference: chr 4
allele count: 3
allele frequency: 2.510460251046025e-5
allele num: 119500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.338G>A
  hgvsp: ENST00000508666.1:c.338G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1005G>A
  hgvsp: ENST00000394706.3:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1122G>A
  hgvsp: ENST00000394708.2:c.1122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1122G>A
  hgvsp: ENST00000273980.5:c.1122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*761G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1122G>A
  hgvsp: ENST00000432496.2:c.1122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.933G>A
  hgvsp: ENST00000361687.4:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.775G>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser374Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

4-107163676-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163676
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163676
    reference: chr 4
allele count: 1
allele frequency: 8.369321415419637e-6
allele num: 119484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*760C>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1121C>G
  hgvsp: ENSP00000273980.4:p.Ser374Trp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1004C>G
  hgvsp: ENSP00000378196.3:p.Ser335Trp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.774C>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1121C>G
  hgvsp: ENSP00000405847.2:p.Ser374Trp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.932C>G
  hgvsp: ENSP00000355338.4:p.Ser311Trp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1121C>G
  hgvsp: ENSP00000378198.2:p.Ser374Trp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.337C>G
  hgvsp: ENSP00000422160.1:p.Ser113Trp
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser374Trp
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ

4-107163678-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163678
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163678
    reference: chr 4
allele count: 1
allele frequency: 8.371002846140968e-6
allele num: 119460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*758C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1119C>T
  hgvsp: ENST00000394708.2:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1119C>T
  hgvsp: ENST00000432496.2:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.335C>T
  hgvsp: ENST00000508666.1:c.335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1119C>T
  hgvsp: ENST00000273980.5:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.1002C>T
  hgvsp: ENST00000394706.3:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.930C>T
  hgvsp: ENST00000361687.4:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.772C>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13519
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser373Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/4-107163682-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163682
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163682
    reference: chr 4
allele count: 1
allele frequency: 8.378437253883405e-6
allele num: 119354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*754G>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1115G>T
  hgvsp: ENSP00000378198.2:p.Arg372Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.998G>T
  hgvsp: ENSP00000378196.3:p.Arg333Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.926G>T
  hgvsp: ENSP00000355338.4:p.Arg309Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.768G>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1115G>T
  hgvsp: ENSP00000405847.2:p.Arg372Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1115G>T
  hgvsp: ENSP00000273980.4:p.Arg372Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.331G>T
  hgvsp: ENSP00000422160.1:p.Arg111Ile
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg372Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

4-107163685-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163685
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163685
    reference: chr 4
allele count: 1
allele frequency: 8.380684199058012e-6
allele num: 119322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.995A>G
  hgvsp: ENSP00000378196.3:p.Asp332Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1112A>G
  hgvsp: ENSP00000378198.2:p.Asp371Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*751A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1112A>G
  hgvsp: ENSP00000273980.4:p.Asp371Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1112A>G
  hgvsp: ENSP00000405847.2:p.Asp371Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.765A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.923A>G
  hgvsp: ENSP00000355338.4:p.Asp308Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.328A>G
  hgvsp: ENSP00000422160.1:p.Asp110Gly
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp371Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/4-107163688-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163688
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163688
    reference: chr 4
allele count: 1
allele frequency: 8.388839487945237e-6
allele num: 119206
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1109G>T
  hgvsp: ENSP00000273980.4:p.Arg370Leu
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.325G>T
  hgvsp: ENSP00000422160.1:p.Arg109Leu
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1109G>T
  hgvsp: ENSP00000378198.2:p.Arg370Leu
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*748G>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.920G>T
  hgvsp: ENSP00000355338.4:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.992G>T
  hgvsp: ENSP00000378196.3:p.Arg331Leu
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.762G>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1109G>T
  hgvsp: ENSP00000405847.2:p.Arg370Leu
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg370Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

4-107163698-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163698
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163698
    reference: chr 4
allele count: 1
allele frequency: 8.427439743805831e-6
allele num: 118660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1099G>A
  hgvsp: ENSP00000378198.2:p.Gly367Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.752G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1099G>A
  hgvsp: ENSP00000273980.4:p.Gly367Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.910G>A
  hgvsp: ENSP00000355338.4:p.Gly304Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1099G>A
  hgvsp: ENSP00000405847.2:p.Gly367Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.315G>A
  hgvsp: ENSP00000422160.1:p.Gly106Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.982G>A
  hgvsp: ENSP00000378196.3:p.Gly328Arg
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*738G>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50411
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4000
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly367Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ

4-107163709-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163709
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163709
    reference: chr 4
allele count: 2
allele frequency: 1.699668564629897e-5
allele num: 117670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.304G>C
  hgvsp: ENSP00000422160.1:p.Gly102Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1088G>C
  hgvsp: ENSP00000405847.2:p.Gly363Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.741G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.971G>C
  hgvsp: ENSP00000378196.3:p.Gly324Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.899G>C
  hgvsp: ENSP00000355338.4:p.Gly300Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1088G>C
  hgvsp: ENSP00000378198.2:p.Gly363Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*727G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1088G>C
  hgvsp: ENSP00000273980.4:p.Gly363Ala
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly363Ala
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

4-107163709-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163709
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163709
    reference: chr 4
allele count: 1
allele frequency: 8.498342823149486e-6
allele num: 117670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.304G>A
  hgvsp: ENSP00000422160.1:p.Gly102Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1088G>A
  hgvsp: ENSP00000378198.2:p.Gly363Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.741G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*727G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.971G>A
  hgvsp: ENSP00000378196.3:p.Gly324Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1088G>A
  hgvsp: ENSP00000405847.2:p.Gly363Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.899G>A
  hgvsp: ENSP00000355338.4:p.Gly300Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1088G>A
  hgvsp: ENSP00000273980.4:p.Gly363Asp
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly363Asp
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-107163711-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163711
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163711
    reference: chr 4
allele count: 1
allele frequency: 8.538980445734779e-6
allele num: 117110
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1086T>C
  hgvsp: ENST00000273980.5:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.897T>C
  hgvsp: ENST00000361687.4:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1086T>C
  hgvsp: ENST00000432496.2:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1086T>C
  hgvsp: ENST00000394708.2:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.739T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.969T>C
  hgvsp: ENST00000394706.3:c.969T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.302T>C
  hgvsp: ENST00000508666.1:c.302T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*725T>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp362Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-107163716-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163716
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163715
    reference: chr 4
allele count: 1
allele frequency: 8.637965586345104e-6
allele num: 115768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1080delT
  hgvsp: ENSP00000405847.2:p.Phe360LeufsTer17
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.296delT
  hgvsp: ENSP00000422160.1:p.Phe99LeufsTer17
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1080delT
  hgvsp: ENSP00000378198.2:p.Phe360LeufsTer17
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.891delT
  hgvsp: ENSP00000355338.4:p.Phe297LeufsTer17
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1080delT
  hgvsp: ENSP00000273980.4:p.Phe360LeufsTer17
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*719delT
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.733delT
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.963delT
  hgvsp: ENSP00000378196.3:p.Phe321LeufsTer17
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe360LeufsTer17
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: CA
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

4-107163721-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163721
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163721
    reference: chr 4
allele count: 1
allele frequency: 8.879575201122378e-6
allele num: 112618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1076T>C
  hgvsp: ENSP00000378198.2:p.Leu359Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1076T>C
  hgvsp: ENSP00000405847.2:p.Leu359Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.729T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1076T>C
  hgvsp: ENSP00000273980.4:p.Leu359Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.292T>C
  hgvsp: ENSP00000422160.1:p.Leu98Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*715T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.887T>C
  hgvsp: ENSP00000355338.4:p.Leu296Pro
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.959T>C
  hgvsp: ENSP00000378196.3:p.Leu320Pro
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu359Pro
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-107163728-TGAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163728
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163723
    reference: chr 4
allele count: 2
allele frequency: 1.868425477849816e-5
allele num: 107042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-7_954-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-7_1071-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-7_1071-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-7_287-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-7_*710-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-7_1071-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-7_882-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-7_724-3delTTTTC
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8477
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 36296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1071-7_1071-3delTTTTC
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: TGAAAA
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

4-107163731-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163731
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163731
    reference: chr 4
allele count: 2
allele frequency: 1.899443463065322e-5
allele num: 105294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-5T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-5T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-5T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-5T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-5T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-5T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-5T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-5T>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1071-5T>C
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

4-107163742-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163742
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163742
    reference: chr 4
allele count: 1
allele frequency: 1.043884922126185e-5
allele num: 95796
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-16A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-16A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-16A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-16A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-16A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-16A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-16A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-16A>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19837
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3286
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

4-107163748-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163748
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163748
    reference: chr 4
allele count: 1
allele frequency: 1.079610476540064e-5
allele num: 92626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-22A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-22A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-22A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-22A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-22A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-22A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-22A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-22A>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24807
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15363
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

4-107163753-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163753
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163753
    reference: chr 4
allele count: 3
allele frequency: 3.359612972585558e-5
allele num: 89296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-27A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23445
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5519
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4813
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24884
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-107163757-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163757
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163757
    reference: chr 4
allele count: 1
allele frequency: 1.175226231049477e-5
allele num: 85090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-31G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-31G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-31G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-31G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-31G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-31G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-31G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-31G>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7291
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23502
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-107163763-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163763
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163763
    reference: chr 4
allele count: 1
allele frequency: 1.240941129752804e-5
allele num: 80584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-37T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-37T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-37T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-37T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-37T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-37T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-37T>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-37T>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9337
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6835
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21204
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2438
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6148
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

4-107163773-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163773
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163773
    reference: chr 4
allele count: 4542
allele frequency: 6.378675954273516e-2
allele num: 71206
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1071-47A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.287-47A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1071-47A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.724-47A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*710-47A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.882-47A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1071-47A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.954-47A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.25e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.75e1
  variant carriers: 258
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18550
  bin: 1.25e1
  variant carriers: 2023
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 2.5e0
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 9528
  bin: 1.75e1
  variant carriers: 1110
genotype depth: GenotypeDepth
  all individuals: 18079
  bin: 7.5e0
  variant carriers: 1564
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 2.25e1
  variant carriers: 499
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 13821
  bin: 2.25e1
  variant carriers: 109
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 4.25e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 5723
  bin: 9.75e1
  variant carriers: 4574
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 2.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 6105
  bin: 3.25e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 6.25e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 176
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.75e1
  variant carriers: 115
num of homozygotes: 175
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

4-107163776-TTTCTTCTAGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107163776
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107163766
    reference: chr 4
allele count: 1
allele frequency: 1.452601609482583e-5
allele num: 68842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7560
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4816
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6558
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: TTTCTTCTAGA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-107165739-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165739
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165739
    reference: chr 4
allele count: 1
allele frequency: 9.858821673633567e-6
allele num: 101432
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1070+44A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.881+44A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.286+44A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1070+44A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.953+44A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1070+44A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*709+44A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.723+44A>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15782
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5069
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3095
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7067
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

4-107165739-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165739
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165739
    reference: chr 4
allele count: 1
allele frequency: 9.858821673633567e-6
allele num: 101432
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1070+44A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.723+44A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.286+44A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*709+44A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.881+44A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.953+44A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1070+44A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1070+44A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8312
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3095
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15551
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

4-107165747-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165747
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165747
    reference: chr 4
allele count: 1
allele frequency: 9.725734292939117e-6
allele num: 102820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.953+36A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.881+36A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1070+36A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*709+36A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1070+36A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1070+36A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.286+36A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.723+36A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22635
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4258
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7428
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22910
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

4-107165758-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165758
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165758
    reference: chr 4
allele count: 1
allele frequency: 9.104317267248129e-6
allele num: 109838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.953+25A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1070+25A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1070+25A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*709+25A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.881+25A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1070+25A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.723+25A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.286+25A>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31988
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4186
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

4-107165759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165759
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165759
    reference: chr 4
allele count: 1
allele frequency: 9.050920478612675e-6
allele num: 110486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1070+24G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1070+24G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*709+24G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.953+24G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1070+24G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.286+24G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.723+24G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.881+24G>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1652
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4864
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

4-107165773-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165773
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165773
    reference: chr 4
allele count: 1
allele frequency: 8.601114704465699e-6
allele num: 116264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.286+10G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1070+10G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*709+10G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.723+10G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.953+10G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1070+10G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1070+10G>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.881+10G>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38453
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5582
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

4-107165775-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165775
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165775
    reference: chr 4
allele count: 1
allele frequency: 8.564136820649846e-6
allele num: 116766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*709+8A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1070+8A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1070+8A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1070+8A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.286+8A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.953+8A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.881+8A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.723+8A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5633
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1070+8A>G
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

4-107165788-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165788
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165788
    reference: chr 4
allele count: 1
allele frequency: 8.394191219675984e-6
allele num: 119130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1065C>G
  hgvsp: ENST00000394708.2:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.948C>G
  hgvsp: ENST00000394706.3:c.948C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1065C>G
  hgvsp: ENST00000273980.5:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.281C>G
  hgvsp: ENST00000508666.1:c.281C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.718C>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1065C>G
  hgvsp: ENST00000432496.2:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*704C>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.876C>G
  hgvsp: ENST00000361687.4:c.876C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu355Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

4-107165794-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165794
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165794
    reference: chr 4
allele count: 4
allele frequency: 3.341129301703976e-5
allele num: 119720
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.712C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1059C>T
  hgvsp: ENST00000273980.5:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1059C>T
  hgvsp: ENST00000394708.2:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.275C>T
  hgvsp: ENST00000508666.1:c.275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*698C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1059C>T
  hgvsp: ENST00000432496.2:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.870C>T
  hgvsp: ENST00000361687.4:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.942C>T
  hgvsp: ENST00000394706.3:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4197
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys353Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-107165800-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165800
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165800
    reference: chr 4
allele count: 1
allele frequency: 8.312690152787244e-6
allele num: 120298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1053T>C
  hgvsp: ENST00000394708.2:c.1053T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*692T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1053T>C
  hgvsp: ENST00000273980.5:c.1053T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.936T>C
  hgvsp: ENST00000394706.3:c.936T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1053T>C
  hgvsp: ENST00000432496.2:c.1053T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.864T>C
  hgvsp: ENST00000361687.4:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.706T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.269T>C
  hgvsp: ENST00000508666.1:c.269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro351Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

4-107165807-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165807
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165807
    reference: chr 4
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.857A>C
  hgvsp: ENSP00000355338.4:p.Lys286Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.699A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*685A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1046A>C
  hgvsp: ENSP00000378198.2:p.Lys349Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.262A>C
  hgvsp: ENSP00000422160.1:p.Lys88Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1046A>C
  hgvsp: ENSP00000273980.4:p.Lys349Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.929A>C
  hgvsp: ENSP00000378196.3:p.Lys310Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1046A>C
  hgvsp: ENSP00000405847.2:p.Lys349Thr
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11756
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys349Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD

4-107165814-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165814
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165814
    reference: chr 4
allele count: 1
allele frequency: 8.278693953241936e-6
allele num: 120792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*678C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1039C>T
  hgvsp: ENSP00000378198.2:p.Arg347Ter
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1039C>T
  hgvsp: ENSP00000405847.2:p.Arg347Ter
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1039C>T
  hgvsp: ENSP00000273980.4:p.Arg347Ter
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.255C>T
  hgvsp: ENSP00000422160.1:p.Arg86Ter
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.850C>T
  hgvsp: ENSP00000355338.4:p.Arg284Ter
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.692C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.922C>T
  hgvsp: ENSP00000378196.3:p.Arg308Ter
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg347Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

4-107165824-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165824
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165824
    reference: chr 4
allele count: 2
allele frequency: 1.653111155194075e-5
allele num: 120984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.245G>A
  hgvsp: ENST00000508666.1:c.245G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.682G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.840G>A
  hgvsp: ENST00000361687.4:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*668G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1029G>A
  hgvsp: ENST00000273980.5:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1029G>A
  hgvsp: ENST00000432496.2:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1029G>A
  hgvsp: ENST00000394708.2:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.912G>A
  hgvsp: ENST00000394706.3:c.912G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2442
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys343Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

4-107165829-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165829
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165829
    reference: chr 4
allele count: 1
allele frequency: 8.263506701703935e-6
allele num: 121014
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.835A>G
  hgvsp: ENSP00000355338.4:p.Asn279Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.240A>G
  hgvsp: ENSP00000422160.1:p.Asn81Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1024A>G
  hgvsp: ENSP00000378198.2:p.Asn342Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.677A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1024A>G
  hgvsp: ENSP00000273980.4:p.Asn342Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.907A>G
  hgvsp: ENSP00000378196.3:p.Asn303Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1024A>G
  hgvsp: ENSP00000405847.2:p.Asn342Asp
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*663A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1920
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5986
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn342Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-107165832-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165832
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165832
    reference: chr 4
allele count: 1
allele frequency: 8.262414277451872e-6
allele num: 121030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*660G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.674G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.904G>A
  hgvsp: ENSP00000378196.3:p.Val302Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.1021G>A
  hgvsp: ENSP00000273980.4:p.Val341Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.832G>A
  hgvsp: ENSP00000355338.4:p.Val278Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.237G>A
  hgvsp: ENSP00000422160.1:p.Val80Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.1021G>A
  hgvsp: ENSP00000378198.2:p.Val341Ile
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.1021G>A
  hgvsp: ENSP00000405847.2:p.Val341Ile
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val341Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

4-107165873-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165873
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165873
    reference: chr 4
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.633A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*178A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.791A>G
  hgvsp: ENSP00000355338.4:p.Tyr264Cys
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.980A>G
  hgvsp: ENSP00000273980.4:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.980A>G
  hgvsp: ENSP00000405847.2:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.196A>G
  hgvsp: ENSP00000422160.1:p.Tyr66Cys
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.980A>G
  hgvsp: ENSP00000378198.2:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*619A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.863A>G
  hgvsp: ENSP00000378196.3:p.Tyr288Cys
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr327Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS

4-107165878-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165878
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165878
    reference: chr 4
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.975G>A
  hgvsp: ENST00000394708.2:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.628G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.975G>A
  hgvsp: ENST00000432496.2:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*173G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.191G>A
  hgvsp: ENST00000508666.1:c.191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.858G>A
  hgvsp: ENST00000394706.3:c.858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.786G>A
  hgvsp: ENST00000361687.4:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.975G>A
  hgvsp: ENST00000273980.5:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*614G>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val325Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-107165879-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165879
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165879
    reference: chr 4
allele count: 167
allele frequency: 1.379686389848152e-3
allele num: 121042
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.974T>C
  hgvsp: ENSP00000273980.4:p.Val325Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.974T>C
  hgvsp: ENSP00000378198.2:p.Val325Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.974T>C
  hgvsp: ENSP00000405847.2:p.Val325Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.857T>C
  hgvsp: ENSP00000378196.3:p.Val286Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*172T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.190T>C
  hgvsp: ENSP00000422160.1:p.Val64Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*613T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.785T>C
  hgvsp: ENSP00000355338.4:p.Val262Ala
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.627T>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 37170
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 4334
  bin: 9.75e1
  variant carriers: 166
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val325Ala
num of homozygotes: 1
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

4-107165889-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165889
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165889
    reference: chr 4
allele count: 2
allele frequency: 1.654916757687088e-5
allele num: 120852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*162A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*603A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.964A>G
  hgvsp: ENSP00000273980.4:p.Ile322Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.964A>G
  hgvsp: ENSP00000405847.2:p.Ile322Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.847A>G
  hgvsp: ENSP00000378196.3:p.Ile283Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.180A>G
  hgvsp: ENSP00000422160.1:p.Ile61Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.964A>G
  hgvsp: ENSP00000378198.2:p.Ile322Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.775A>G
  hgvsp: ENSP00000355338.4:p.Ile259Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.617A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile322Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

4-107165893-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165893
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165893
    reference: chr 4
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.960A>C
  hgvsp: ENSP00000405847.2:p.Arg320Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.176A>C
  hgvsp: ENSP00000422160.1:p.Arg59Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.613A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.771A>C
  hgvsp: ENSP00000355338.4:p.Arg257Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.960A>C
  hgvsp: ENSP00000273980.4:p.Arg320Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*599A>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.843A>C
  hgvsp: ENSP00000378196.3:p.Arg281Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.960A>C
  hgvsp: ENSP00000378198.2:p.Arg320Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*158A>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4190
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg320Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

4-107165909-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165909
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165909
    reference: chr 4
allele count: 1
allele frequency: 8.364141253617491e-6
allele num: 119558
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*142A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.944A>G
  hgvsp: ENSP00000405847.2:p.Asp315Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.160A>G
  hgvsp: ENSP00000422160.1:p.Asp54Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.597A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.827A>G
  hgvsp: ENSP00000378196.3:p.Asp276Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*583A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.944A>G
  hgvsp: ENSP00000378198.2:p.Asp315Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.944A>G
  hgvsp: ENSP00000273980.4:p.Asp315Gly
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.755A>G
  hgvsp: ENSP00000355338.4:p.Asp252Gly
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp315Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

4-107165912-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165912
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165912
    reference: chr 4
allele count: 63
allele frequency: 5.278592375366569e-4
allele num: 119350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*580A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.941A>G
  hgvsp: ENSP00000378198.2:p.Asn314Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*139A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.752A>G
  hgvsp: ENSP00000355338.4:p.Asn251Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.941A>G
  hgvsp: ENSP00000405847.2:p.Asn314Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.157A>G
  hgvsp: ENSP00000422160.1:p.Asn53Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.941A>G
  hgvsp: ENSP00000273980.4:p.Asn314Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.594A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.824A>G
  hgvsp: ENSP00000378196.3:p.Asn275Ser
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11768
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35244
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn314Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-107165915-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165915
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165915
    reference: chr 4
allele count: 1
allele frequency: 8.41609156707625e-6
allele num: 118820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.749A>G
  hgvsp: ENSP00000355338.4:p.Asn250Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.821A>G
  hgvsp: ENSP00000378196.3:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.938A>G
  hgvsp: ENSP00000378198.2:p.Asn313Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.938A>G
  hgvsp: ENSP00000273980.4:p.Asn313Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.938A>G
  hgvsp: ENSP00000405847.2:p.Asn313Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.591A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.154A>G
  hgvsp: ENSP00000422160.1:p.Asn52Ser
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*136A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*577A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn313Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

4-107165918-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165918
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165918
    reference: chr 4
allele count: 5
allele frequency: 4.214003978019755e-5
allele num: 118652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.818T>C
  hgvsp: ENSP00000378196.3:p.Ile273Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.151T>C
  hgvsp: ENSP00000422160.1:p.Ile51Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.935T>C
  hgvsp: ENSP00000378198.2:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.588T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.935T>C
  hgvsp: ENSP00000405847.2:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.746T>C
  hgvsp: ENSP00000355338.4:p.Ile249Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*133T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.935T>C
  hgvsp: ENSP00000273980.4:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*574T>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39000
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile312Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

4-107165919-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165919
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165919
    reference: chr 4
allele count: 3
allele frequency: 2.529425651748676e-5
allele num: 118604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.745A>G
  hgvsp: ENSP00000355338.4:p.Ile249Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.934A>G
  hgvsp: ENSP00000405847.2:p.Ile312Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.150A>G
  hgvsp: ENSP00000422160.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*132A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.934A>G
  hgvsp: ENSP00000273980.4:p.Ile312Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*573A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.817A>G
  hgvsp: ENSP00000378196.3:p.Ile273Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.934A>G
  hgvsp: ENSP00000378198.2:p.Ile312Val
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.587A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile312Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-107165932-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165932
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165932
    reference: chr 4
allele count: 39
allele frequency: 3.329861170403511e-4
allele num: 117122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-11G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-11G>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32286
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11065
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1838
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4225
  bin: 9.75e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 5513
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

4-107165942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165942
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165942
    reference: chr 4
allele count: 102
allele frequency: 8.863091307219075e-4
allele num: 115084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-21C>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-21C>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28799
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6472
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10364
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5330
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-107165944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165944
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165944
    reference: chr 4
allele count: 22
allele frequency: 1.918314673363329e-4
allele num: 114684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-23T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-23T>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27939
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

4-107165947-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165947
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165947
    reference: chr 4
allele count: 2
allele frequency: 1.763699536147022e-5
allele num: 113398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-26T>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-26T>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

4-107165948-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165948
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165948
    reference: chr 4
allele count: 2
allele frequency: 1.763512917732122e-5
allele num: 113410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-27A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-27A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4185
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1797
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

4-107165955-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165955
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165955
    reference: chr 4
allele count: 2
allele frequency: 1.780183002812689e-5
allele num: 112348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-34T>C
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-34T>C
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9536
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8921
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4931
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

4-107165956-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165956
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165956
    reference: chr 4
allele count: 3
allele frequency: 2.681923833363133e-5
allele num: 111860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-35A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-35A>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2329
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4890
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

4-107165958-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165958
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165958
    reference: chr 4
allele count: 2
allele frequency: 1.805999530440122e-5
allele num: 110742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-37A>T
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-37A>T
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22969
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

4-107165961-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165961
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165961
    reference: chr 4
allele count: 3
allele frequency: 2.725092653150207e-5
allele num: 110088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000421182
  ensembl transcript: ENST00000467183
  gene symbol: TBCK
  hgvsc: ENST00000467183.2:c.*571-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000355338
  ensembl transcript: ENST00000361687
  gene symbol: TBCK
  hgvsc: ENST00000361687.4:c.743-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378196
  ensembl transcript: ENST00000394706
  gene symbol: TBCK
  hgvsc: ENST00000394706.3:c.815-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-40A>G
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000273980
  ensembl transcript: ENST00000273980
  gene symbol: TBCK
  hgvsc: ENST00000273980.5:c.932-40A>G
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8869
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3692
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21868
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

4-107165965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107165965
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 107165965
    reference: chr 4
allele count: 1
allele frequency: 9.199293494259642e-6
allele num: 108704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000422160
  ensembl transcript: ENST00000508666
  gene symbol: TBCK
  hgvsc: ENST00000508666.1:c.148-44G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000378198
  ensembl transcript: ENST00000394708
  gene symbol: TBCK
  hgvsc: ENST00000394708.2:c.932-44G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000426093
  ensembl transcript: ENST00000505574
  gene symbol: TBCK
  hgvsc: ENST00000505574.1:c.*130-44G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl protein: ENSP00000405847
  ensembl transcript: ENST00000432496
  gene symbol: TBCK
  hgvsc: ENST00000432496.2:c.932-44G>A
  variant of: http://identifiers.org/hgnc/28261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145348
  ensembl transcript: ENST00000510927
  gene symbol: TBCK
  hgvsc: ENST00000510927.1:n.585-44G>A
  variant of: http://identifiers.org/hgnc/28261
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 188
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3935
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531675039823551e-5
allele num: 65288
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.455407e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.369e0

VQSLOD
type: SiteQuality
SIO_000300: -2.209e0

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.106e0

QD
type: SiteQuality
SIO_000300: 5.87e0

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

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3954
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528724737823707e-5
allele num: 65414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166316771635176e-4
allele num: 8574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.132e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 9.859999999999999e0

DP
type: SiteQuality
SIO_000300: 1.460909e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.117e1

VQSLOD
type: SiteQuality
SIO_000300: -2.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50878
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4007
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.196554715578138e-5
allele num: 16138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.593e0

FS
type: SiteQuality
SIO_000300: 3.544e0

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

DP
type: SiteQuality
SIO_000300: 1.461635e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4007
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 50878
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.196554715578138e-5
allele num: 16138
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525832341542311e-5
allele num: 65538
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

FS
type: SiteQuality
SIO_000300: 3.544e0

QD
type: SiteQuality
SIO_000300: 1.292e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.593e0

DP
type: SiteQuality
SIO_000300: 1.461635e6

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 51101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.046551303923958e-5
allele num: 65648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

FS
type: SiteQuality
SIO_000300: 3.184e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

QD
type: SiteQuality
SIO_000300: 1.223e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.106e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.464786e6

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51170
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 462
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.043398867855621e-5
allele num: 65716
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11268
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.799e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

QD
type: SiteQuality
SIO_000300: 1.436e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.649e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.74e-1

DP
type: SiteQuality
SIO_000300: 1.466018e6

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 9.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.559963520291838e-5
allele num: 65790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 1.834e0

DP
type: SiteQuality
SIO_000300: 1.467889e6

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.77e-1

QD
type: SiteQuality
SIO_000300: 1.103e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 51350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.922603691208574e-5
allele num: 10078
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65790
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 1.467889e6

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.77e-1

QD
type: SiteQuality
SIO_000300: 1.103e1

FS
type: SiteQuality
SIO_000300: 1.834e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51320
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.157635467980295e-5
allele num: 16240
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65782
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.238e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

DP
type: SiteQuality
SIO_000300: 1.468076e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.869e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

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

GenotypeQuality
all individuals: 453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
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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: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518003521768171e-5
allele num: 65876
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.285e0

FS
type: SiteQuality
SIO_000300: 9.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.47049e6

VQSLOD
type: SiteQuality
SIO_000300: 4.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.106e1

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
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GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 70
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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: 28
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518187890933382e-5
allele num: 65868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.585e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.470419e6

VQSLOD
type: SiteQuality
SIO_000300: -3.995e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.73e-1

FS
type: SiteQuality
SIO_000300: 1.992e0

QD
type: SiteQuality
SIO_000300: 1.09e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.856e0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
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variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 51309
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 2.25e1
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 1602
bin: 9.75e1
variant carriers: 256

GenotypeQuality
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GenotypeQuality
all individuals: 740
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 200
allele frequency: 3.03702128951924e-3
allele num: 65854
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163873370577281e-4
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.916089451810805e-4
allele num: 10106
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.423995752964077e-4
allele num: 11302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 27
allele frequency: 4.120879120879121e-3
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.595284872298625e-4
allele num: 16288
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.169e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.481404e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 168
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51851064475962e-5
allele num: 65854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.481404e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

QD
type: SiteQuality
SIO_000300: 1.169e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
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GenotypeQuality
all individuals: 4071
bin: 6.75e1
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GenotypeQuality
all individuals: 239
bin: 9.25e1
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GenotypeQuality
all individuals: 441
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GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.27859638462707e-4
allele num: 65830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.143260842855388e-5
allele num: 16278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.054367745876604e-4
allele num: 6548
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 1.471284e6

GenotypeQuality
all individuals: 441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 168
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GenotypeQuality
all individuals: 1094
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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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: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
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GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038128512836093e-5
allele num: 65830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10070
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

DP
type: SiteQuality
SIO_000300: 1.471284e6

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

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

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51418
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
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GenotypeQuality
all individuals: 1375
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variant carriers: 3

GenotypeQuality
all individuals: 441
bin: 8.25e1
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GenotypeQuality
all individuals: 168
bin: 8.75e1
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GenotypeQuality
all individuals: 4071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.557192769254139e-5
allele num: 65830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

FS
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 1.471284e6

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 1114
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
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GenotypeQuality
all individuals: 1353
bin: 9.75e1
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GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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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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bin: 5.75e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.144015728680265e-5
allele num: 16276
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65814
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

QD
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SIO_000300: 6.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.981e0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.058e0

InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.470455e6

FS
type: SiteQuality
SIO_000300: 4.945e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.85112409275978e-5
allele num: 11298
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65796
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.1328e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.904e1

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.489e0

DP
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SIO_000300: 1.470058e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

VQSLOD
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SIO_000300: -1.718e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
SIO_000300: 1.08e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521051350693599e-5
allele num: 65744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.501e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
SIO_000300: 7.152e0

DP
type: SiteQuality
SIO_000300: 1.468988e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.960159362549801e-5
allele num: 10040
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

QD
type: SiteQuality
SIO_000300: 3.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e-1

FS
type: SiteQuality
SIO_000300: 7.68e-1

DP
type: SiteQuality
SIO_000300: 1.468557e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

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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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65656
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.976057462090982e-5
allele num: 10024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 8.33e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.256e0

MQRankSum
type: SiteQuality
SIO_000300: -8.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.365e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.44e0

DP
type: SiteQuality
SIO_000300: 1.467561e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529660109523664e-5
allele num: 65374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.946e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.460128e6

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

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

African
type: Population
allele count: 2
allele frequency: 2.050861361771944e-4
allele num: 9752
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64786
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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InbreedingCoeff
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MQ
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.446145e6

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.232082762059081e-5
allele num: 16046
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64786
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.551831160769708e-5
allele num: 64440
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

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

Other
type: Population
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allele num: 874
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.93e0

FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQ
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.436791e6

MQRankSum
type: SiteQuality
SIO_000300: -1.044e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.072763563781528e-5
allele num: 11022
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

DP
type: SiteQuality
SIO_000300: 1.418465e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.063e0

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

FS
type: SiteQuality
SIO_000300: 7.171e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
all individuals: 416
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 43
bin: 4.25e1
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GenotypeQuality
all individuals: 145
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.626862757857747e-5
allele num: 61468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

FS
type: SiteQuality
SIO_000300: 2.169e0

DP
type: SiteQuality
SIO_000300: 1.368599e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.35e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeQuality
all individuals: 114
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 219
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variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15178
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.461165720614703e-5
allele num: 57784
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.021e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.616e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 7.073e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 5.463e1

DP
type: SiteQuality
SIO_000300: 1.282229e6

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
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variant carriers: 0

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

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.528830545557202e-5
allele num: 56676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15024
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.407e0

FS
type: SiteQuality
SIO_000300: 3.431e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

QD
type: SiteQuality
SIO_000300: 1.709e1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.411e0

DP
type: SiteQuality
SIO_000300: 1.25063e6

GenotypeQuality
all individuals: 364
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1349
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variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.968426439903941e-5
allele num: 50802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.873e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 1.65e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.5e-3

DP
type: SiteQuality
SIO_000300: 1.059258e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

GenotypeQuality
all individuals: 576
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 256
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4292
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variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48828
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.272727272727273e-5
allele num: 13750
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.562e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

DP
type: SiteQuality
SIO_000300: 9.86671e5

QD
type: SiteQuality
SIO_000300: 1.118e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 221
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9498
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.2294887039239e-4
allele num: 13456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6898
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.252e-1

DP
type: SiteQuality
SIO_000300: 9.25531e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.533e0

FS
type: SiteQuality
SIO_000300: 7.92e0

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6299
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.274277916761428e-5
allele num: 43970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.367e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.164e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.15e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

DP
type: SiteQuality
SIO_000300: 8.77648e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.942811755361398e-5
allele num: 12590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5838
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: 668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5216
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.552e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.35763e5

GenotypeQuality
all individuals: 3731
bin: 1.25e1
variant carriers: 49

GenotypeQuality
all individuals: 1856
bin: 4.75e1
variant carriers: 65

GenotypeQuality
all individuals: 272
bin: 7.25e1
variant carriers: 25

GenotypeQuality
all individuals: 6035
bin: 7.5e0
variant carriers: 34

GenotypeQuality
all individuals: 616
bin: 6.75e1
variant carriers: 43

GenotypeQuality
all individuals: 3972
bin: 3.75e1
variant carriers: 41

GenotypeQuality
all individuals: 402
bin: 7.75e1
variant carriers: 71

GenotypeQuality
all individuals: 5524
bin: 1.75e1
variant carriers: 73

GenotypeQuality
all individuals: 4412
bin: 2.75e1
variant carriers: 72

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 130

GenotypeQuality
all individuals: 402
bin: 9.25e1
variant carriers: 216

GenotypeQuality
all individuals: 923
bin: 5.25e1
variant carriers: 108

Other
type: Population
allele count: 43
allele frequency: 7.142857142857142e-2
allele num: 602
num of homozygotes: 2

Latino
type: Population
allele count: 250
allele frequency: 3.058478101296795e-2
allele num: 8174
num of homozygotes: 5

African
type: Population
allele count: 305
allele frequency: 5.396319886765746e-2
allele num: 5652
num of homozygotes: 8

South Asian
type: Population
allele count: 362
allele frequency: 3.09295967190704e-2
allele num: 11704
num of homozygotes: 6

East Asian
type: Population
allele count: 1
allele frequency: 1.954652071931196e-4
allele num: 5116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3269
allele frequency: 9.284294234592445e-2
allele num: 35210
num of homozygotes: 140

European (Finnish)
type: Population
allele count: 312
allele frequency: 6.571187868576242e-2
allele num: 4748
num of homozygotes: 14

QD
type: SiteQuality
SIO_000300: 1.758e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

DP
type: SiteQuality
SIO_000300: 7.97531e5

VQSLOD
type: SiteQuality
SIO_000300: 5.77e0

GenotypeQuality
all individuals: 4321
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6822
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4444
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.735150244584206e-5
allele num: 11448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.58e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.095e0

MQ
type: SiteQuality
SIO_000300: 4.164e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.531e0

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.130000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-1

DP
type: SiteQuality
SIO_000300: 7.86709e5

GenotypeQuality
all individuals: 4163
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2053
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5236
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.388503193557345e-4
allele num: 7202
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

QD
type: SiteQuality
SIO_000300: 1.28e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.258716e6

GenotypeQuality
all individuals: 4163
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5236
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5069
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4137
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.766409948420829e-5
allele num: 56612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

DP
type: SiteQuality
SIO_000300: 1.258716e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

QD
type: SiteQuality
SIO_000300: 1.28e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

GenotypeQuality
all individuals: 324
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4173
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
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: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.437e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 1.329907e6

MQ
type: SiteQuality
SIO_000300: 5.884e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

QD
type: SiteQuality
SIO_000300: 1.528e1

GenotypeQuality
all individuals: 231
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1545
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.630470227613644e-5
allele num: 61332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12502
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.366e0

QD
type: SiteQuality
SIO_000300: 1.507e1

DP
type: SiteQuality
SIO_000300: 1.455041e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.267e0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.6e-1

MQ
type: SiteQuality
SIO_000300: 5.82e1

GenotypeQuality
all individuals: 140
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5212
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34260
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 692
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.620325361332556e-5
allele num: 61716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.539e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.706e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 9.26e0

DP
type: SiteQuality
SIO_000300: 1.465475e6

GenotypeQuality
all individuals: 2405
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540072691431036e-5
allele num: 64932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.765e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

VQSLOD
type: SiteQuality
SIO_000300: 8.19e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.532821e6

QD
type: SiteQuality
SIO_000300: 1.388e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
all individuals: 711
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.114399544678429e-5
allele num: 14056
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65162
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.479e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

DP
type: SiteQuality
SIO_000300: 1.537467e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.42e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

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

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

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5796
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4193
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.064e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.123e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.567341e6

FS
type: SiteQuality
SIO_000300: 5.904e0

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.37e0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41237
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.550044625780951e-4
allele num: 15686
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66180
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

FS
type: SiteQuality
SIO_000300: 3.858e0

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.656e0

DP
type: SiteQuality
SIO_000300: 1.575481e6

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4194
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2434
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.112e0

DP
type: SiteQuality
SIO_000300: 1.582439e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeQuality
all individuals: 349
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5927
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41983
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.156877231867996e-5
allele num: 16242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.559e-1

DP
type: SiteQuality
SIO_000300: 1.586042e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.401e0

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.796999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.533e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 1.590083e6

MQ
type: SiteQuality
SIO_000300: 5.924e1

QD
type: SiteQuality
SIO_000300: 8.19e0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4193
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 719
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42440
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.858e1

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

DP
type: SiteQuality
SIO_000300: 1.59134e6

FS
type: SiteQuality
SIO_000300: 2.229e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.328e-1

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42451
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2439
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
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: 16452
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

FS
type: SiteQuality
SIO_000300: 5.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.21e-1

QD
type: SiteQuality
SIO_000300: 1.158e1

DP
type: SiteQuality
SIO_000300: 1.591889e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.15e-1

GenotypeQuality
all individuals: 2433
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42477
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5992
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 717
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variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
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: 16460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 2.051e0

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.014999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.288e0

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

DP
type: SiteQuality
SIO_000300: 1.592031e6

GenotypeQuality
all individuals: 171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5988
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 716
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.816e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.999e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 1.591923e6

FS
type: SiteQuality
SIO_000300: 9.45e-1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5984
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.294e0

VQSLOD
type: SiteQuality
SIO_000300: -1.547e0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.609e0

FS
type: SiteQuality
SIO_000300: 1.827e0

MQ
type: SiteQuality
SIO_000300: 5.851e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

QD
type: SiteQuality
SIO_000300: 1.442e1

DP
type: SiteQuality
SIO_000300: 1.591748e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5958
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.750087504375219e-4
allele num: 11428
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.848374061958822e-4
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 123
allele frequency: 1.846846846846847e-3
allele num: 66600
num of homozygotes: 1

South Asian
type: Population
allele count: 38
allele frequency: 2.308066083576287e-3
allele num: 16464
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

DP
type: SiteQuality
SIO_000300: 1.600922e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.29e-2

FS
type: SiteQuality
SIO_000300: 5.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.288e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 4191
bin: 9.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 42092
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GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.589654e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.171e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

FS
type: SiteQuality
SIO_000300: 1.309e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5959
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GenotypeQuality
all individuals: 471
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

FS
type: SiteQuality
SIO_000300: 1.472e0

MQ
type: SiteQuality
SIO_000300: 5.909e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

DP
type: SiteQuality
SIO_000300: 1.588347e6

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4190
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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
all individuals: 2403
bin: 7.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512035805007863e-5
allele num: 66136
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.567517e6

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.637e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.639e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 63

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.434178355424013e-5
allele num: 15542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.270319358256395e-4
allele num: 66070
num of homozygotes: 0

African
type: Population
allele count: 46
allele frequency: 4.486054222742344e-3
allele num: 10254
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65896
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16333178222429e-4
allele num: 8596
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10188
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.84e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 1.345e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 2.011e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15212
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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allele num: 880
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European (Finnish)
type: Population
allele count: 4
allele frequency: 6.073489219556636e-4
allele num: 6586
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519064256418047e-5
allele num: 65830
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.55001e6

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 3.032e0

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

QD
type: SiteQuality
SIO_000300: 1.525e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
all individuals: 164
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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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: 5.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.163873370577281e-4
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.966568338249754e-4
allele num: 10170
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.26e0

FS
type: SiteQuality
SIO_000300: 1.717e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 1.648e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.08e-1

DP
type: SiteQuality
SIO_000300: 1.549912e6

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 201
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GenotypeQuality
all individuals: 1685
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 2.653422234317594e-3
allele num: 14698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
SIO_000300: 4.227e0

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

DP
type: SiteQuality
SIO_000300: 1.518898e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.282e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 102

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
all individuals: 1814
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variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14264
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.09849157054126e-4
allele num: 11270
num of homozygotes: 0

African
type: Population
allele count: 88
allele frequency: 8.988764044943821e-3
allele num: 9790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.17096018735363e-3
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.808595702148926e-5
allele num: 64032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.334e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 1.473307e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.28e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-1

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 31427
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GenotypeQuality
all individuals: 713
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63818
num of homozygotes: 0

South Asian
type: Population
allele count: 22
allele frequency: 1.548859476203886e-3
allele num: 14204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.460313e6

FS
type: SiteQuality
SIO_000300: 1.263e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.65e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
all individuals: 1783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2336
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.094240837696335e-4
allele num: 9550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13918
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.551e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: -3.672e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.431767e6

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-1

GenotypeQuality
all individuals: 2001
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 710
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GenotypeQuality
all individuals: 168
bin: 4.75e1
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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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13912
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.418964683115626e-4
allele num: 8268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.430883e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.17e0

QD
type: SiteQuality
SIO_000300: 1.674e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 713
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.955758552749418e-5
allele num: 11166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.05708245243129e-4
allele num: 9460
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.528e1

DP
type: SiteQuality
SIO_000300: 1.403926e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 1.217e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

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

GenotypeQuality
all individuals: 410
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GenotypeQuality
all individuals: 497
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8746
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GenotypeQuality
all individuals: 2251
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1764
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GenotypeQuality
all individuals: 413
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GenotypeQuality
all individuals: 349
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GenotypeQuality
all individuals: 1674
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GenotypeQuality
all individuals: 4185
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 25091
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.811702059408481e-5
allele num: 62348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13560
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.403e1

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 1.435e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

DP
type: SiteQuality
SIO_000300: 1.395203e6

GenotypeQuality
all individuals: 2318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2416
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4706
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.004141905276428e-5
allele num: 11106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8112
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.074806534823732e-4
allele num: 9304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.63e1

VQSLOD
type: SiteQuality
SIO_000300: -8.092e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.592e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.380805e6

GenotypeQuality
all individuals: 713
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8094
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.586102260658473e-5
allele num: 13182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.25754120789628e-5
allele num: 61396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 6.131e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 1.526e1

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 1.372708e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1