18-12324936-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324936
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324936
    reference: chr 18
allele count: 1
allele frequency: 1.279525040305039e-5
allele num: 78154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*189G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*115G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12176G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.278-30G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-130G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-130G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13884G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4209G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-130G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-130G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-130G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-130G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-130G>C
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15399
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

18-12324943-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324943
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324943
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 79990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-123C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*122C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12169C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-123C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13891C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.278-23C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-123C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-123C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-123C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-123C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4202C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-123C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

18-12324950-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324950
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324950
    reference: chr 18
allele count: 23
allele frequency: 2.680340286679874e-4
allele num: 85810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-116T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-116T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-116T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*203T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.278-16T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*129T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13898T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-116T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-116T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-116T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-116T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4195T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12162T>G
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26609
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

18-12324954-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324954
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324954
    reference: chr 18
allele count: 1
allele frequency: 1.128006136353382e-5
allele num: 88652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-112T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.278-12T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-112T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*133T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*207T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13902T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-112T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12158T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-112T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-112T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4191T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-112T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-112T>G
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29355
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

18-12324963-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324963
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324963
    reference: chr 18
allele count: 3
allele frequency: 3.149937001259975e-5
allele num: 95240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-103C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13911C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-103C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-103C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-103C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12149C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-103C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.278-3C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4182C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*216C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-103C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-103C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.278-3C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

18-12324966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324966
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324966
    reference: chr 18
allele count: 1
allele frequency: 1.031225508394176e-5
allele num: 96972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-100C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4179C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13914C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.278C>T
  hgvsp: ENSP00000467969.1:p.Ala93Val
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*145C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12146C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-100C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-100C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-100C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*219C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-100C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-100C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-100C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34875
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala93Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-12324968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324968
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324968
    reference: chr 18
allele count: 1
allele frequency: 1.019742209169522e-5
allele num: 98064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.280C>T
  hgvsp: ENSP00000467969.1:p.His94Tyr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*221C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-98C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13916C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*147C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-98C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-98C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4177C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-98C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-98C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12144C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-98C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-98C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His94Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

18-12324971-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324971
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324971
    reference: chr 18
allele count: 400
allele frequency: 4.020181310177089e-3
allele num: 99498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-95C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-95C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-95C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-95C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13919C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*224C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12141C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-95C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*150C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-95C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.283C>G
  hgvsp: ENSP00000467969.1:p.His95Asp
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4174C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-95C>G
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 35901
  bin: 2.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 2.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.His95Asp
num of homozygotes: 9
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP

18-12324971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324971
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324971
    reference: chr 18
allele count: 1
allele frequency: 1.005045327544272e-5
allele num: 99498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13919C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-95C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4174C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12141C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-95C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*150C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-95C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*224C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-95C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-95C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.283C>T
  hgvsp: ENSP00000467969.1:p.His95Tyr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-95C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-95C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His95Tyr
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

18-12324979-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324979
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324979
    reference: chr 18
allele count: 15
allele frequency: 1.469349372098035e-4
allele num: 102086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-87C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*232C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12133C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.291C>T
  hgvsp: ENST00000592683.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*158C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-87C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-87C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4166C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-87C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-87C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13927C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-87C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-87C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36934
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ile97Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

18-12324980-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324980
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324980
    reference: chr 18
allele count: 3
allele frequency: 2.925402242808386e-5
allele num: 102550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4165A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12132A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-86A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-86A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-86A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*233A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-86A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*159A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-86A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13928A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.292A>G
  hgvsp: ENSP00000467969.1:p.Thr98Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-86A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-86A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr98Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

18-12324992-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324992
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324992
    reference: chr 18
allele count: 3
allele frequency: 2.866588950255126e-5
allele num: 104654
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-74C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*245C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12120C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-74C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-74C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.304C>T
  hgvsp: ENSP00000467969.1:p.Pro102Ser
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-74C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-74C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-74C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-74C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*171C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4153C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13940C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro102Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

18-12324998-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324998
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324998
    reference: chr 18
allele count: 13
allele frequency: 1.234356900055071e-4
allele num: 105318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.310C>G
  hgvsp: ENSP00000467969.1:p.Arg104Gly
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4147C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-68C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12114C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-68C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-68C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*177C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13946C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*251C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-68C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-68C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-68C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-68C>G
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg104Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

18-12324999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12324999
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12324999
    reference: chr 18
allele count: 27
allele frequency: 2.557399408956581e-4
allele num: 105576
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-67G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4146G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.311G>A
  hgvsp: ENSP00000467969.1:p.Arg104Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*252G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*178G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-67G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-67G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-67G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-67G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-67G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-67G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13947G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12113G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38119
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg104Gln
num of homozygotes: 1
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-12325007-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325007
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325007
    reference: chr 18
allele count: 1
allele frequency: 9.392317084624776e-6
allele num: 106470
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-59A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-59A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*186A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*260A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-59A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13955A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-59A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12105A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*4A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4138A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-59A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-59A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-59A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

18-12325011-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325011
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325012
    reference: chr 18
allele count: 1
allele frequency: 9.349813938702619e-6
allele num: 106954
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-53dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*192dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13961dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4132dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-53dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*10dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-53dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*266dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-53dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12099dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-53dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-53dupG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-53dupG
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

18-12325014-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325014
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325014
    reference: chr 18
allele count: 1
allele frequency: 9.330447115025753e-6
allele num: 107176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12098T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4131T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-52T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-52T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*267T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*11T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13962T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-52T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*193T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-52T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-52T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-52T>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-52T>G
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

18-12325020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325020
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325020
    reference: chr 18
allele count: 1
allele frequency: 9.287638153617536e-6
allele num: 107670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12092C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-46C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-46C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4125C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-46C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*199C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-46C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13968C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-46C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-46C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-46C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

18-12325021-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325021
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325021
    reference: chr 18
allele count: 1788
allele frequency: 1.656936335835418e-2
allele num: 107910
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-45G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*200G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*274G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-45G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-45G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-45G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13969G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*18G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-45G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-45G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-45G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12091G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4124G>C
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 7.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 533
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 37771
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 2.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 82
genotype quality: GenotypeQuality
num of homozygotes: 25
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

18-12325021-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325021
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325021
    reference: chr 18
allele count: 30
allele frequency: 2.780094523213789e-4
allele num: 107910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13969G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12091G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-45G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-45G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-45G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-45G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-45G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*200G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*18G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4124G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-45G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-45G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*274G>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11137
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

18-12325033-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325033
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325032
    reference: chr 18
allele count: 1
allele frequency: 9.194218675296973e-6
allele num: 108764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-32delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-32delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*213delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*287delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-32delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4111delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-32delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*31delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-32delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-32delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-32delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12078delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13982delG
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: TG
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

18-12325034-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325034
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325034
    reference: chr 18
allele count: 2
allele frequency: 1.837762340574117e-5
allele num: 108828
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12078G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-32G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-32G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-32G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*213G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-32G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-32G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-32G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*287G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13982G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4111G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-32G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*31G>C
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

18-12325041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325041
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325041
    reference: chr 18
allele count: 2
allele frequency: 1.834357516279923e-5
allele num: 109030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4104C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-25C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-25C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13989C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*294C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-25C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-25C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-25C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12071C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*220C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-25C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-25C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

18-12325042-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325042
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325042
    reference: chr 18
allele count: 11
allele frequency: 1.007861318282604e-4
allele num: 109142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-24G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12070G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-24G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+13990G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-24G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*295G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*221G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4103G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-24G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-24G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-24G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-24G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12224
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

18-12325050-ACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325050
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325048
    reference: chr 18
allele count: 1
allele frequency: 9.121258003903899e-6
allele num: 109634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4090_278-4089delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*61-11_*61-10delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.278-11_278-10delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.278-11_278-10delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.278-11_278-10delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*308_*309delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.62-11_62-10delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.167-11_167-10delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12057_278-12056delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*234_*235delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.667-11_667-10delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14003_87+14004delCT
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*52_*53delCT
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: ACT
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

18-12325074-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325074
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325074
    reference: chr 18
allele count: 1
allele frequency: 9.043226623259178e-6
allele num: 110580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.286G>C
  hgvsp: ENSP00000466849.1:p.Gly96Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*253G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.175G>C
  hgvsp: ENSP00000468777.1:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.70G>C
  hgvsp: ENSP00000468571.1:p.Gly24Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.286G>C
  hgvsp: ENSP00000318697.4:p.Gly96Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*327G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.286G>C
  hgvsp: ENSP00000465891.1:p.Gly96Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14022G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*71G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12038G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*69G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.675G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4071G>C
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly96Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

18-12325075-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325075
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325075
    reference: chr 18
allele count: 1
allele frequency: 9.040773890245005e-6
allele num: 110610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.287G>C
  hgvsp: ENSP00000465891.1:p.Gly96Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.287G>C
  hgvsp: ENSP00000466849.1:p.Gly96Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*70G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.71G>C
  hgvsp: ENSP00000468571.1:p.Gly24Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*254G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12037G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.287G>C
  hgvsp: ENSP00000318697.4:p.Gly96Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.176G>C
  hgvsp: ENSP00000468777.1:p.Gly59Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*72G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14023G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4070G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*328G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.676G>C
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12530
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly96Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

18-12325077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325077
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325077
    reference: chr 18
allele count: 1
allele frequency: 9.031628763931287e-6
allele num: 110722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.73G>A
  hgvsp: ENSP00000468571.1:p.Ala25Thr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*72G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.289G>A
  hgvsp: ENSP00000318697.4:p.Ala97Thr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4068G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*74G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.289G>A
  hgvsp: ENSP00000465891.1:p.Ala97Thr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.178G>A
  hgvsp: ENSP00000468777.1:p.Ala60Thr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.289G>A
  hgvsp: ENSP00000466849.1:p.Ala97Thr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*256G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.678G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*330G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12035G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14025G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala97Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

18-12325080-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325080
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325080
    reference: chr 18
allele count: 1
allele frequency: 9.022827754218172e-6
allele num: 110830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*75G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14028G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.681G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.76G>C
  hgvsp: ENSP00000468571.1:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4065G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*333G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.292G>C
  hgvsp: ENSP00000465891.1:p.Gly98Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.292G>C
  hgvsp: ENSP00000466849.1:p.Gly98Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*77G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.292G>C
  hgvsp: ENSP00000318697.4:p.Gly98Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*259G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12032G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.181G>C
  hgvsp: ENSP00000468777.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly98Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

18-12325081-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325081
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325081
    reference: chr 18
allele count: 1
allele frequency: 9.020711553727359e-6
allele num: 110856
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.293G>T
  hgvsp: ENSP00000318697.4:p.Gly98Val
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*260G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.293G>T
  hgvsp: ENSP00000465891.1:p.Gly98Val
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.293G>T
  hgvsp: ENSP00000466849.1:p.Gly98Val
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.182G>T
  hgvsp: ENSP00000468777.1:p.Gly61Val
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4064G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12031G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.682G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.77G>T
  hgvsp: ENSP00000468571.1:p.Gly26Val
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*334G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14029G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*76G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*78G>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly98Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

18-12325082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325082
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325082
    reference: chr 18
allele count: 1
allele frequency: 9.01859634566476e-6
allele num: 110882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*79G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.183G>A
  hgvsp: ENST00000590103.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4063G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.294G>A
  hgvsp: ENST00000317702.5:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.683G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*77G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*335G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.294G>A
  hgvsp: ENST00000590693.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.78G>A
  hgvsp: ENST00000591463.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*261G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14030G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12030G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.294G>A
  hgvsp: ENST00000591208.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly98Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

18-12325100-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325100
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325100
    reference: chr 18
allele count: 2
allele frequency: 1.790093621896425e-5
allele num: 111726
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*97G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*353G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.312G>T
  hgvsp: ENST00000317702.5:c.312G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.312G>T
  hgvsp: ENST00000590693.1:c.312G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.311+1G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*279G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.201G>T
  hgvsp: ENST00000590103.1:c.201G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14048G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.701G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.96G>T
  hgvsp: ENST00000591463.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12012G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*95G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4045G>T
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.311+1G>T
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: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

18-12325102-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325102
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325102
    reference: chr 18
allele count: 1
allele frequency: 8.931123178050872e-6
allele num: 111968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.314A>G
  hgvsp: ENSP00000465891.1:p.His105Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*97A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.98A>G
  hgvsp: ENSP00000468571.1:p.His33Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.314A>G
  hgvsp: ENSP00000318697.4:p.His105Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.203A>G
  hgvsp: ENSP00000468777.1:p.His68Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12010A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.703A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*281A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*355A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.311+3A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14050A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4043A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*99A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His105Arg
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

18-12325109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325109
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325109
    reference: chr 18
allele count: 4
allele frequency: 3.556124535481233e-5
allele num: 112482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.311+10G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*288G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.321G>A
  hgvsp: ENST00000317702.5:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.105G>A
  hgvsp: ENST00000591463.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-12003G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*362G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14057G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4036G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.710G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*104G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.321G>A
  hgvsp: ENST00000590693.1:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.210G>A
  hgvsp: ENST00000590103.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*106G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr107Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-12325115-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325115
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325115
    reference: chr 18
allele count: 1
allele frequency: 8.858337467224152e-6
allele num: 112888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*294C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.327C>A
  hgvsp: ENST00000317702.5:c.327C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.311+16C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14063C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11997C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*110C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.216C>A
  hgvsp: ENST00000590103.1:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.111C>A
  hgvsp: ENST00000591463.1:c.111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*368C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467969
  ensembl transcript: ENST00000592683
  gene symbol: TUBB6
  hgvsc: ENST00000592683.1:c.*112C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.327C>A
  hgvsp: ENST00000590693.1:c.327C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4030C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.716C>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly109Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

18-12325133-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325133
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325133
    reference: chr 18
allele count: 1
allele frequency: 8.631404502140589e-6
allele num: 115856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*128A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.311+34A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.345A>G
  hgvsp: ENST00000590693.1:c.345A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.234A>G
  hgvsp: ENST00000590103.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*312A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.129A>G
  hgvsp: ENST00000591463.1:c.129A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.734A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*386A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4012A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.345A>G
  hgvsp: ENST00000317702.5:c.345A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11979A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14081A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala115Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

18-12325139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325139
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325139
    reference: chr 18
allele count: 1
allele frequency: 8.567365192508696e-6
allele num: 116722
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.351G>A
  hgvsp: ENST00000317702.5:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.351G>A
  hgvsp: ENST00000590693.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*134G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*392G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*318G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11973G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14087G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.311+40G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.135G>A
  hgvsp: ENST00000591463.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4006G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.240G>A
  hgvsp: ENST00000590103.1:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.740G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu117Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

18-12325140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325140
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325140
    reference: chr 18
allele count: 2
allele frequency: 1.711596063329054e-5
allele num: 116850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.241G>A
  hgvsp: ENSP00000468777.1:p.Asp81Asn
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.136G>A
  hgvsp: ENSP00000468571.1:p.Asp46Asn
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.311+41G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11972G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.352G>A
  hgvsp: ENSP00000465891.1:p.Asp118Asn
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.741G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14088G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*135G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.352G>A
  hgvsp: ENSP00000318697.4:p.Asp118Asn
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4005G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*393G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*319G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp118Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

18-12325142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325142
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325142
    reference: chr 18
allele count: 1173
allele frequency: 1.001314598876616e-2
allele num: 117146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.312-40C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.354C>T
  hgvsp: ENST00000317702.5:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14090C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.243C>T
  hgvsp: ENST00000590103.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*321C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-4003C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.138C>T
  hgvsp: ENST00000591463.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.354C>T
  hgvsp: ENST00000590693.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*137C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11970C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*395C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.743C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12858
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40030
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 805
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
hgvs: p.Asp118Asp
num of homozygotes: 7
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

18-12325150-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325150
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325150
    reference: chr 18
allele count: 2
allele frequency: 1.686454398273071e-5
allele num: 118592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11962G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3995G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.312-32G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*329G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*145G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*403G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14098G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.362G>A
  hgvsp: ENSP00000318697.4:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.146G>A
  hgvsp: ENSP00000468571.1:p.Arg49Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.251G>A
  hgvsp: ENSP00000468777.1:p.Arg84Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.751G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.362G>A
  hgvsp: ENSP00000465891.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/18-12325152-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325152
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325152
    reference: chr 18
allele count: 1
allele frequency: 8.416941620092923e-6
allele num: 118808
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.148A>C
  hgvsp: ENSP00000468571.1:p.Lys50Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3993A>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.253A>C
  hgvsp: ENSP00000468777.1:p.Lys85Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.364A>C
  hgvsp: ENSP00000318697.4:p.Lys122Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.312-30A>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*405A>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.364A>C
  hgvsp: ENSP00000465891.1:p.Lys122Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11960A>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.753A>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*331A>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*147A>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14100A>C
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys122Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

18-12325173-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325173
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325172
    reference: chr 18
allele count: 1
allele frequency: 8.29462508294625e-6
allele num: 120560
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.386delG
  hgvsp: ENSP00000318697.4:p.Cys129SerfsTer36
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*353delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*427delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14122delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.386delG
  hgvsp: ENSP00000465891.1:p.Cys129SerfsTer?
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.275delG
  hgvsp: ENSP00000468777.1:p.Cys92SerfsTer36
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11938delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.170delG
  hgvsp: ENSP00000468571.1:p.Cys57SerfsTer36
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.775delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*169delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3971delG
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.312-8delG
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys129SerfsTer36
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: TG
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/18-12325175-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325175
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325175
    reference: chr 18
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.387C>A
  hgvsp: ENSP00000318697.4:p.Cys129Ter
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14123C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.276C>A
  hgvsp: ENSP00000468777.1:p.Cys92Ter
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3970C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*354C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465891
  ensembl transcript: ENST00000590693
  gene symbol: TUBB6
  hgvsc: ENST00000590693.1:c.387C>A
  hgvsp: ENSP00000465891.1:p.Cys129Ter
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.171C>A
  hgvsp: ENSP00000468571.1:p.Cys57Ter
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*170C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.312-7C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*428C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.776C>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11937C>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys129Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

18-12325194-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325194
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325194
    reference: chr 18
allele count: 1
allele frequency: 8.264326209484141e-6
allele num: 121002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*447A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468179
  ensembl transcript: ENST00000590388
  gene symbol: TUBB6
  hgvsc: ENST00000590388.1:c.*189A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.190A>G
  hgvsp: ENSP00000468571.1:p.Thr64Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.795A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.295A>G
  hgvsp: ENSP00000468777.1:p.Thr99Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.324A>G
  hgvsp: ENST00000591208.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11918A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.406A>G
  hgvsp: ENSP00000318697.4:p.Thr136Ala
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3951A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*373A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14142A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr136Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

18-12325202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325202
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325202
    reference: chr 18
allele count: 187
allele frequency: 1.544458943821338e-3
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.803G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*381G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.198G>A
  hgvsp: ENST00000591463.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11910G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.303G>A
  hgvsp: ENST00000590103.1:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*455G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.332G>A
  hgvsp: ENSP00000466849.1:p.Arg111His
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3943G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14150G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.414G>A
  hgvsp: ENST00000317702.5:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 41265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 14564
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg111His
num of homozygotes: 2
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

18-12325217-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325217
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325217
    reference: chr 18
allele count: 3
allele frequency: 2.476596166229135e-5
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*470G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.347G>A
  hgvsp: ENSP00000466849.1:p.Arg116Gln
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.318G>A
  hgvsp: ENST00000590103.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11895G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3928G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.429G>A
  hgvsp: ENST00000317702.5:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14165G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.213G>A
  hgvsp: ENST00000591463.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.818G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*396G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14891
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg116Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

18-12325235-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325235
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325235
    reference: chr 18
allele count: 11
allele frequency: 9.067528356634133e-5
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3910G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.336G>A
  hgvsp: ENST00000590103.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14183G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.365G>A
  hgvsp: ENSP00000466849.1:p.Arg122His
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11877G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*488G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*414G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.231G>A
  hgvsp: ENST00000591463.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.447G>A
  hgvsp: ENST00000317702.5:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.836G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg122His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

18-12325245-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325245
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325245
    reference: chr 18
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*498A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.375A>G
  hgvsp: ENST00000591208.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.457A>G
  hgvsp: ENSP00000318697.4:p.Ser153Gly
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.846A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3900A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*424A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11867A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.346A>G
  hgvsp: ENSP00000468777.1:p.Ser116Gly
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.241A>G
  hgvsp: ENSP00000468571.1:p.Ser81Gly
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14193A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser153Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

18-12325254-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325254
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325254
    reference: chr 18
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.355C>T
  hgvsp: ENSP00000468777.1:p.Arg119Cys
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.250C>T
  hgvsp: ENSP00000468571.1:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14202C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11858C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*507C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.384C>T
  hgvsp: ENST00000591208.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.466C>T
  hgvsp: ENSP00000318697.4:p.Arg156Cys
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3891C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*433C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.855C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg156Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

18-12325259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325259
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325259
    reference: chr 18
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.389G>A
  hgvsp: ENSP00000466849.1:p.Arg130Lys
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.471G>A
  hgvsp: ENST00000317702.5:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3886G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.360G>A
  hgvsp: ENST00000590103.1:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.860G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*438G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*512G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14207G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.255G>A
  hgvsp: ENST00000591463.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11853G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg130Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

18-12325265-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325265
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325265
    reference: chr 18
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.866C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.366C>G
  hgvsp: ENSP00000468777.1:p.Phe122Leu
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.477C>G
  hgvsp: ENSP00000318697.4:p.Phe159Leu
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468820
  ensembl transcript: ENST00000586653
  gene symbol: TUBB6
  hgvsc: ENST00000586653.1:c.*444C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*518C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11847C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.395C>G
  hgvsp: ENSP00000466849.1:p.Ser132Cys
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14213C>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.261C>G
  hgvsp: ENSP00000468571.1:p.Phe87Leu
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3880C>G
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4977
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Phe159Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

18-12325273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325273
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325273
    reference: chr 18
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11839G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14221G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.485G>A
  hgvsp: ENSP00000318697.4:p.Arg162His
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.269G>A
  hgvsp: ENSP00000468571.1:p.Arg90His
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.403G>A
  hgvsp: ENSP00000466849.1:p.Ala135Thr
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.374G>A
  hgvsp: ENSP00000468777.1:p.Arg125His
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.874G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3872G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*526G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg162His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

18-12325283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325283
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325283
    reference: chr 18
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3862C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.279C>T
  hgvsp: ENST00000591463.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.495C>T
  hgvsp: ENST00000317702.5:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.384C>T
  hgvsp: ENST00000590103.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.884C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*536C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14231C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11829C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn165Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

18-12325292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325292
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325292
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.893C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.288C>T
  hgvsp: ENST00000591463.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.504C>T
  hgvsp: ENST00000317702.5:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*545C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.393C>T
  hgvsp: ENST00000590103.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3853C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11820C>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14240C>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser168Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

18-12325293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325293
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325293
    reference: chr 18
allele count: 15
allele frequency: 1.235523779714347e-4
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*546G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.289G>A
  hgvsp: ENSP00000468571.1:p.Val97Ile
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.505G>A
  hgvsp: ENSP00000318697.4:p.Val169Ile
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14241G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11819G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.894G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.394G>A
  hgvsp: ENSP00000468777.1:p.Val132Ile
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3852G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val169Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

18-12325309-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325309
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325309
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14257A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11803A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.305A>G
  hgvsp: ENSP00000468571.1:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.410A>G
  hgvsp: ENSP00000468777.1:p.Lys137Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.521A>G
  hgvsp: ENSP00000318697.4:p.Lys174Arg
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3836A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.910A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*28A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*562A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys174Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

18-12325316-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325316
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325316
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.417G>A
  hgvsp: ENST00000590103.1:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11796G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.528G>A
  hgvsp: ENST00000317702.5:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14264G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*569G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.312G>A
  hgvsp: ENST00000591463.1:c.312G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.917G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3829G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41041
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser176Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

18-12325320-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325320
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325320
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.532A>T
  hgvsp: ENSP00000318697.4:p.Thr178Ser
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*573A>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.316A>T
  hgvsp: ENSP00000468571.1:p.Thr106Ser
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3825A>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.921A>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.421A>T
  hgvsp: ENSP00000468777.1:p.Thr141Ser
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14268A>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11792A>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*39A>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr178Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

18-12325325-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325325
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325325
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14273G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.426G>T
  hgvsp: ENST00000590103.1:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*44G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.321G>T
  hgvsp: ENST00000591463.1:c.321G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3820G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.926G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.537G>T
  hgvsp: ENST00000317702.5:c.537G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*578G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11787G>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val179Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

18-12325326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325326
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325326
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.538G>A
  hgvsp: ENSP00000318697.4:p.Val180Met
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14274G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*579G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.322G>A
  hgvsp: ENSP00000468571.1:p.Val108Met
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.427G>A
  hgvsp: ENSP00000468777.1:p.Val143Met
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*45G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.927G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11786G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3819G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val180Met
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: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

18-12325328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325328
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325328
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.324G>A
  hgvsp: ENST00000591463.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.540G>A
  hgvsp: ENST00000317702.5:c.540G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.429G>A
  hgvsp: ENST00000590103.1:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.929G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3817G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*581G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14276G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*47G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11784G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val180Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

18-12325339-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325339
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325339
    reference: chr 18
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*58A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11773A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*592A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3806A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.440A>G
  hgvsp: ENSP00000468777.1:p.Asn147Ser
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14287A>G
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.335A>G
  hgvsp: ENSP00000468571.1:p.Asn112Ser
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.551A>G
  hgvsp: ENSP00000318697.4:p.Asn184Ser
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.940A>G
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn184Ser
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: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-12325352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325352
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325352
    reference: chr 18
allele count: 184
allele frequency: 1.515700682065307e-3
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.453G>A
  hgvsp: ENST00000590103.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11760G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14300G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3793G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.953G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.348G>A
  hgvsp: ENST00000591463.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*605G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.564G>A
  hgvsp: ENST00000317702.5:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*71G>A
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser188Ser
num of homozygotes: 3
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

18-12325352-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325352
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325352
    reference: chr 18
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468571
  ensembl transcript: ENST00000591463
  gene symbol: TUBB6
  hgvsc: ENST00000591463.1:c.348G>C
  hgvsp: ENST00000591463.1:c.348G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14300G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11760G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.564G>C
  hgvsp: ENST00000317702.5:c.564G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.953G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*605G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3793G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.453G>C
  hgvsp: ENST00000590103.1:c.453G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*71G>C
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser188Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

18-12325353-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325353
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325353
    reference: chr 18
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.954G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.565G>T
  hgvsp: ENSP00000318697.4:p.Val189Leu
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3792G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*606G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.454G>T
  hgvsp: ENSP00000468777.1:p.Val152Leu
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11759G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*72G>T
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14301G>T
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val189Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

18-12325365-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325365
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325365
    reference: chr 18
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11747G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3780G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*618G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.577G>C
  hgvsp: ENSP00000318697.4:p.Val193Leu
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.966G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.466G>C
  hgvsp: ENSP00000468777.1:p.Val156Leu
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14313G>C
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*84G>C
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val193Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

18-12325370-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325370
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325370
    reference: chr 18
allele count: 646
allele frequency: 5.321339725530898e-3
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465040
  ensembl transcript: ENST00000591909
  gene symbol: TUBB6
  hgvsc: ENST00000591909.1:c.278-3775G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000467348
  ensembl transcript: ENST00000586810
  gene symbol: TUBB6
  hgvsc: ENST00000586810.1:c.*623G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465386
  ensembl transcript: ENST00000590967
  gene symbol: TUBB6
  hgvsc: ENST00000590967.1:c.278-11742G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000465448
  ensembl transcript: ENST00000586691
  gene symbol: TUBB6
  hgvsc: ENST00000586691.1:c.87+14318G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000318697
  ensembl transcript: ENST00000317702
  gene symbol: TUBB6
  hgvsc: ENST00000317702.5:c.582G>A
  hgvsp: ENST00000317702.5:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000466849
  ensembl transcript: ENST00000591208
  gene symbol: TUBB6
  hgvsc: ENST00000591208.1:c.*89G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176014
  ensembl transcript: ENST00000417736
  gene symbol: TUBB6
  hgvsc: ENST00000417736.2:n.971G>A
  variant of: http://identifiers.org/hgnc/20776
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176014
  ensembl protein: ENSP00000468777
  ensembl transcript: ENST00000590103
  gene symbol: TUBB6
  hgvsc: ENST00000590103.1:c.471G>A
  hgvsp: ENST00000590103.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20776
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 601
genotype depth: GenotypeDepth
  all individuals: 40489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 9.75e1
  variant carriers: 640
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu194Glu
num of homozygotes: 6
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

18-12325385-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 12325385
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 12325385
    reference: chr 18
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
canonical: true
consequence: synonymous
filter: PASS
hgvs: p.Thr199Thr
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 5600
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14439
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 752
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4984
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3864
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12358
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6713
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 799
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14035
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45328
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.470155836518671e-4
allele num: 6802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.855e0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.08284e5

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

GenotypeDepth
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 836
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12048
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1308
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18823
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6948
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 8.73748e5

FS
type: SiteQuality
SIO_000300: 2.793e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.174e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 291
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10312
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2502
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 9.75e1
variant carriers: 22

South Asian
type: Population
allele count: 4
allele frequency: 5.402485143165856e-4
allele num: 7404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.883239171374765e-4
allele num: 5310
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.085540599218411e-4
allele num: 9212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 3.431016388148866e-4
allele num: 49548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.608e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.96e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

DP
type: SiteQuality
SIO_000300: 9.88187e5

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31540
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3044
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2313
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7184
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.954804910469935e-5
allele num: 51156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7606
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

DP
type: SiteQuality
SIO_000300: 1.030847e6

QD
type: SiteQuality
SIO_000300: 1.5e1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.43e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

VQSLOD
type: SiteQuality
SIO_000300: -1.22e0

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

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 348
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6245
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 352
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.638877770095702e-5
allele num: 54962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.292657704239917e-4
allele num: 7736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 1.498e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.74e-1

DP
type: SiteQuality
SIO_000300: 1.1239e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.706e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38908
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5482
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.787757437070938e-5
allele num: 55936
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10630
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 2.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.606e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.146141e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

GenotypeDepth
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8898
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2719
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39896
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 218
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5051
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.767346505955958e-5
allele num: 56582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5884
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.741e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.783e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

DP
type: SiteQuality
SIO_000300: 1.159577e6

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

QD
type: SiteQuality
SIO_000300: 1.009e1

GenotypeDepth
all individuals: 26
bin: 5.75e1
variant carriers: 12

GenotypeDepth
all individuals: 1932
bin: 3.25e1
variant carriers: 62

GenotypeDepth
all individuals: 31
bin: 5.25e1
variant carriers: 14

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 703
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 653
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 797
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 658
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 193
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2645
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40537
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3575
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 237
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 358
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 583
bin: 9.75e1
variant carriers: 386

GenotypeQuality
all individuals: 253
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 379
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8006
num of homozygotes: 0

African
type: Population
allele count: 361
allele frequency: 4.385325558794947e-2
allele num: 8232
num of homozygotes: 9

Latino
type: Population
allele count: 26
allele frequency: 2.396755162241888e-3
allele num: 10848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.569092367237351e-4
allele num: 57358
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.890173410404624e-3
allele num: 692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.378686964795433e-4
allele num: 8408
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.49e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

QD
type: SiteQuality
SIO_000300: 1.697e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.180371e6

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 653
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2645
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40537
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.214771622934888e-4
allele num: 8232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8006
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57358
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.49e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.697e1

DP
type: SiteQuality
SIO_000300: 1.180371e6

VQSLOD
type: SiteQuality
SIO_000300: 6.14e0

GenotypeDepth
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 2157
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2490
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3441
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3793
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 9.75e1
variant carriers: 15

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.69940860580518e-5
allele num: 58844
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.404494382022472e-3
allele num: 8544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.807991321641656e-4
allele num: 11062
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.443e1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.062e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

DP
type: SiteQuality
SIO_000300: 1.210565e6

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3888
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 237
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43051
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.07700118463361e-5
allele num: 59090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.437e0

VQSLOD
type: SiteQuality
SIO_000300: -1.182e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.904e0

DP
type: SiteQuality
SIO_000300: 1.214815e6

QD
type: SiteQuality
SIO_000300: 1.448e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeDepth
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44441
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2504
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 261
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.660026560424967e-5
allele num: 60240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.392757660167131e-3
allele num: 718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.127649977447e-4
allele num: 8868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.59e0

VQSLOD
type: SiteQuality
SIO_000300: 9.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 6.165e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

DP
type: SiteQuality
SIO_000300: 1.242381e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 621
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2865
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.145568575672553e-4
allele num: 60590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8898
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 1.251763e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

QD
type: SiteQuality
SIO_000300: 1.667e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

FS
type: SiteQuality
SIO_000300: 3.099e0

VQSLOD
type: SiteQuality
SIO_000300: 5.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3153
bin: 2.5e0
variant carriers: 2

GenotypeDepth
all individuals: 16
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2873
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4149
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.75e1
variant carriers: 26

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

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44943
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.824567596187787e-5
allele num: 11332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

South Asian
type: Population
allele count: 22
allele frequency: 2.470244778800808e-3
allele num: 8906
num of homozygotes: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.724795640326975e-3
allele num: 734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.292831505811848e-5
allele num: 60738
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 1.255214e6

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

QD
type: SiteQuality
SIO_000300: 1.558e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38453
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3083
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4228
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 45470
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.632120124041129e-5
allele num: 61270
num of homozygotes: 0

Latino
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: 748
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

QD
type: SiteQuality
SIO_000300: 1.645e1

DP
type: SiteQuality
SIO_000300: 1.264218e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.374e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.11e0

GenotypeDepth
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1794
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3155
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45709
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61568
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.118568232662192e-4
allele num: 8940
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.05e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

DP
type: SiteQuality
SIO_000300: 1.269005e6

GenotypeDepth
all individuals: 456
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 368
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45755
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.057753331922996e-4
allele num: 9454
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61694
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.758e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 1.41e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

DP
type: SiteQuality
SIO_000300: 1.272105e6

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4288
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.612227130558153e-5
allele num: 62026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8960
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.142e0

VQSLOD
type: SiteQuality
SIO_000300: 9.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.25e-1

DP
type: SiteQuality
SIO_000300: 1.27754e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.66e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 1.288e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeDepth
all individuals: 150
bin: 8.25e1
variant carriers: 144

GenotypeDepth
all individuals: 11137
bin: 2.75e1
variant carriers: 31

GenotypeDepth
all individuals: 155
bin: 7.75e1
variant carriers: 148

GenotypeDepth
all individuals: 2380
bin: 3.25e1
variant carriers: 29

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 10

GenotypeQuality
all individuals: 363
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 9.75e1
variant carriers: 1754

GenotypeQuality
all individuals: 1416
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3217
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 755
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4070
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 44968
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.25e1
variant carriers: 1

Latino
type: Population
allele count: 61
allele frequency: 5.344314000350446e-3
allele num: 11414
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

African
type: Population
allele count: 36
allele frequency: 3.755476736907991e-3
allele num: 9586
num of homozygotes: 0

South Asian
type: Population
allele count: 261
allele frequency: 2.911646586345382e-2
allele num: 8964
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 1391
allele frequency: 2.235903041213914e-2
allele num: 62212
num of homozygotes: 18

Other
type: Population
allele count: 17
allele frequency: 2.225130890052356e-2
allele num: 764
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 22
allele frequency: 3.349573690621194e-3
allele num: 6568
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

VQSLOD
type: SiteQuality
SIO_000300: 5.76e0

DP
type: SiteQuality
SIO_000300: 1.382259e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.529e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

GenotypeDepth
all individuals: 83
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 9.75e1
variant carriers: 12

GenotypeDepth
all individuals: 2380
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 363
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 9.75e1
variant carriers: 30

GenotypeQuality
all individuals: 44968
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3217
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

East Asian
type: Population
allele count: 30
allele frequency: 3.570578433706261e-3
allele num: 8402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

VQSLOD
type: SiteQuality
SIO_000300: 5.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.382259e6

QD
type: SiteQuality
SIO_000300: 1.529e1

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2833
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3691
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 46705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4387
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.59454029403323e-5
allele num: 62714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

QD
type: SiteQuality
SIO_000300: 1.484e1

FS
type: SiteQuality
SIO_000300: 7.427e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQ
type: SiteQuality
SIO_000300: 6.016e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

DP
type: SiteQuality
SIO_000300: 1.300849e6

MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

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

GenotypeDepth
all individuals: 21
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3701
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4389
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.371916508538899e-4
allele num: 8432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.301848e6

FS
type: SiteQuality
SIO_000300: 3.155e0

QD
type: SiteQuality
SIO_000300: 1.378e1

MQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.59e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 142
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3665
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46730
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590229629158451e-5
allele num: 62884
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.013376570733685e-4
allele num: 9868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

FS
type: SiteQuality
SIO_000300: 4.349e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.739e0

QD
type: SiteQuality
SIO_000300: 1.244e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

DP
type: SiteQuality
SIO_000300: 1.306414e6

GenotypeDepth
all individuals: 38455
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 146
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3697
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46868
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.112234580384226e-3
allele num: 9890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

DP
type: SiteQuality
SIO_000300: 1.308593e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

FS
type: SiteQuality
SIO_000300: 4.462e0

QD
type: SiteQuality
SIO_000300: 1.18e1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

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

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1417
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4444
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 88
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3486
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 832
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.105216622458002e-4
allele num: 9048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63248
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.588e1

MQ
type: SiteQuality
SIO_000300: 6.026e1

FS
type: SiteQuality
SIO_000300: 3.7e0

MQRankSum
type: SiteQuality
SIO_000300: -2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.133e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

DP
type: SiteQuality
SIO_000300: 1.31522e6

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

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

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2373
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47587
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 973
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4505
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568233855032463e-5
allele num: 63766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

FS
type: SiteQuality
SIO_000300: 4.284e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.337e0

QD
type: SiteQuality
SIO_000300: 8.74e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.438e0

DP
type: SiteQuality
SIO_000300: 1.331537e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47602
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9288
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567742137773179e-5
allele num: 63786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

QD
type: SiteQuality
SIO_000300: 1.097e1

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.331914e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

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

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47613
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4512
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e-1

FS
type: SiteQuality
SIO_000300: 6.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.013e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.067e0

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1

DP
type: SiteQuality
SIO_000300: 1.33325e6

GenotypeDepth
all individuals: 2115
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2022
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63872
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.173708920187793e-4
allele num: 8520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.572e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 1.297e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.334955e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e-1

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4514
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 354
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47634
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1981
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2571
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63886
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

DP
type: SiteQuality
SIO_000300: 1.335406e6

QD
type: SiteQuality
SIO_000300: 1.587e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

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

GenotypeDepth
all individuals: 21
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12574
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4516
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47643
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1951
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 1.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564896247378799e-5
allele num: 63902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.098e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.453e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.335735e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.108e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

QD
type: SiteQuality
SIO_000300: 6.65e0

GenotypeDepth
all individuals: 621
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2935
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47742
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3252
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.117401334247771e-5
allele num: 64156
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.09e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.345665e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

FS
type: SiteQuality
SIO_000300: 5.588e0

QD
type: SiteQuality
SIO_000300: 1.006e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

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

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3343
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47777
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.780907668231612e-5
allele num: 10224
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64228
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.07e-1

QD
type: SiteQuality
SIO_000300: 1.192e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.347099e6

FS
type: SiteQuality
SIO_000300: 4.191e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.92e-1

GenotypeDepth
all individuals: 827
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 4

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.673989249824726e-4
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.151e1

DP
type: SiteQuality
SIO_000300: 1.352257e6

FS
type: SiteQuality
SIO_000300: 1.134e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 111
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 200
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3493
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47902
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64438
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

QD
type: SiteQuality
SIO_000300: 1.454e1

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

DP
type: SiteQuality
SIO_000300: 1.355307e6

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

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2774
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49183
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 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: 12784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534401276621862e-5
allele num: 65172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

FS
type: SiteQuality
SIO_000300: 8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.37923e6

QD
type: SiteQuality
SIO_000300: 1.562e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

VQSLOD
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeDepth
all individuals: 12980
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2397
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 994
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4640
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 448
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 49590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530221882172915e-5
allele num: 65350
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.840000000000001e-1

FS
type: SiteQuality
SIO_000300: 8.090999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.282e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.908e1

DP
type: SiteQuality
SIO_000300: 1.386939e6

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeDepth
all individuals: 421
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4640
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2348
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 49592
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65376
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13528
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.387984e6

FS
type: SiteQuality
SIO_000300: 4.791e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.742e0

QD
type: SiteQuality
SIO_000300: 1.166e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.91e-1

GenotypeDepth
all individuals: 41
bin: 6.25e1
variant carriers: 29

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 24

GenotypeQuality
all individuals: 233
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 9.75e1
variant carriers: 1164

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

GenotypeQuality
all individuals: 49007
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4487
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 134
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 943
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 30
allele frequency: 2.907540220973057e-3
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.750802451123432e-3
allele num: 13708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 224
allele frequency: 3.389830508474576e-2
allele num: 6608
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 846
allele frequency: 1.292037020067809e-2
allele num: 65478
num of homozygotes: 6

Latino
type: Population
allele count: 42
allele frequency: 3.638884075550164e-3
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 8.009153318077803e-3
allele num: 874
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

DP
type: SiteQuality
SIO_000300: 1.494477e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

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

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4744
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 989
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50668
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518649009840846e-5
allele num: 65848
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.779661016949152e-5
allele num: 14750
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

FS
type: SiteQuality
SIO_000300: 1.167e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.36e1

DP
type: SiteQuality
SIO_000300: 1.409855e6

GenotypeDepth
all individuals: 477
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50759
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 278
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65906
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14906
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: 10342
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.777e1

DP
type: SiteQuality
SIO_000300: 1.411534e6

VQSLOD
type: SiteQuality
SIO_000300: -1.454e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

FS
type: SiteQuality
SIO_000300: 3.453e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

QD
type: SiteQuality
SIO_000300: 1.491e1

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51940
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1045
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66350
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: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16172
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.744e1

FS
type: SiteQuality
SIO_000300: 1.178e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.836e0

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.212e0

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.431632e6

GenotypeDepth
all individuals: 41460
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14264
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 856
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4877
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51939
bin: 6.25e1
variant carriers: 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: 16198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.47e-1

QD
type: SiteQuality
SIO_000300: 1.724e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.43258e6

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.589e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 2.493e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.831e0

VQSLOD
type: SiteQuality
SIO_000300: -1.2e0

GenotypeQuality
all individuals: 4943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 278
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52273
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.438823e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.341e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

MQRankSum
type: SiteQuality
SIO_000300: -2.024e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 9.75e1
variant carriers: 185

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 853
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52120
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 226
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4939
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.222222222222222e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 154
allele frequency: 2.314536491523386e-3
allele num: 66536
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.106362311801845e-4
allele num: 16472
num of homozygotes: 2

African
type: Population
allele count: 2
allele frequency: 1.92789666473877e-4
allele num: 10374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 1.967312348668281e-3
allele num: 6608
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

DP
type: SiteQuality
SIO_000300: 1.449155e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: 5.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

QD
type: SiteQuality
SIO_000300: 1.396e1

GenotypeQuality
all individuals: 1028
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.507482420818559e-5
allele num: 66556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

FS
type: SiteQuality
SIO_000300: 2.488e0

QD
type: SiteQuality
SIO_000300: 1.417e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

DP
type: SiteQuality
SIO_000300: 1.443894e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.17e-1

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1044
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.780346820809249e-4
allele num: 8650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 6
allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-1

QD
type: SiteQuality
SIO_000300: 1.407e1

DP
type: SiteQuality
SIO_000300: 1.448309e6

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

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

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 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: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.37e-1

FS
type: SiteQuality
SIO_000300: 9.550000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.979e0

DP
type: SiteQuality
SIO_000300: 1.448974e6

QD
type: SiteQuality
SIO_000300: 1.215e1

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.538e1

VQSLOD
type: SiteQuality
SIO_000300: -3.074e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.35e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

MQRankSum
type: SiteQuality
SIO_000300: -1.092e0

FS
type: SiteQuality
SIO_000300: 2.413e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-2

DP
type: SiteQuality
SIO_000300: 1.449429e6

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 52816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.554e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.449656e6

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
type: SiteQuality
SIO_000300: 2.872e0

QD
type: SiteQuality
SIO_000300: 1.338e1

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1049
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

DP
type: SiteQuality
SIO_000300: 1.449725e6

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

FS
type: SiteQuality
SIO_000300: 2.218e0

QD
type: SiteQuality
SIO_000300: 1.107e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

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

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

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4978
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52844
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.795e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-2

QD
type: SiteQuality
SIO_000300: 1.177e1

FS
type: SiteQuality
SIO_000300: 3.103e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.449943e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

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

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

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

GenotypeQuality
all individuals: 838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 1

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

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

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

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

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
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: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e0

MQ
type: SiteQuality
SIO_000300: 5.997e1

DP
type: SiteQuality
SIO_000300: 1.450067e6

MQRankSum
type: SiteQuality
SIO_000300: 2.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.414e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.013e0

QD
type: SiteQuality
SIO_000300: 1.453e1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52845
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.014e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.276e1

DP
type: SiteQuality
SIO_000300: 1.450053e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52840
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4975
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.75e1
variant carriers: 15

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.249279261964251e-3
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

QD
type: SiteQuality
SIO_000300: 1.33e1

DP
type: SiteQuality
SIO_000300: 1.451651e6

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52848
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.516e0

QD
type: SiteQuality
SIO_000300: 1.357e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.450504e6

FS
type: SiteQuality
SIO_000300: 5.987e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e0

VQSLOD
type: SiteQuality
SIO_000300: -1.262e0

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4977
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52846
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

FS
type: SiteQuality
SIO_000300: 2.924e0

QD
type: SiteQuality
SIO_000300: 1.257e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

DP
type: SiteQuality
SIO_000300: 1.450521e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

VQSLOD
type: SiteQuality
SIO_000300: -1.098e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4978
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52846
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 1.008e1

FS
type: SiteQuality
SIO_000300: 7.4e-1

DP
type: SiteQuality
SIO_000300: 1.450396e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4980
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52847
bin: 6.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.922e0

DP
type: SiteQuality
SIO_000300: 1.450471e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.909e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.37e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.543e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

QD
type: SiteQuality
SIO_000300: 1.42e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

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

GenotypeQuality
all individuals: 4979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52844
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.394e0

FS
type: SiteQuality
SIO_000300: 3.764e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.381e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-1

DP
type: SiteQuality
SIO_000300: 1.450425e6

MQ
type: SiteQuality
SIO_000300: 5.777e1

MQRankSum
type: SiteQuality
SIO_000300: -1.192e0

VQSLOD
type: SiteQuality
SIO_000300: -2.518e0

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

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4977
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52846
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.835e0

QD
type: SiteQuality
SIO_000300: 8.93e0

VQSLOD
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 1.450395e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.683e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

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

GenotypeQuality
all individuals: 838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52842
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
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: 6614
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.184e1

FS
type: SiteQuality
SIO_000300: 2.551e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

DP
type: SiteQuality
SIO_000300: 1.450662e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

GenotypeQuality
all individuals: 823
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 9.75e1
variant carriers: 181

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

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

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1042
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52720
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 152
allele frequency: 1.757225433526012e-2
allele num: 8650
num of homozygotes: 2

South Asian
type: Population
allele count: 22
allele frequency: 1.332364341085271e-3
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.048972007432716e-4
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.212389380530973e-3
allele num: 904
num of homozygotes: 1

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

DP
type: SiteQuality
SIO_000300: 1.479912e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.33e-2

QD
type: SiteQuality
SIO_000300: 1.369e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

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

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

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1042
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52720
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.33e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.01e-1

DP
type: SiteQuality
SIO_000300: 1.479912e6

QD
type: SiteQuality
SIO_000300: 1.369e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 4979
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.988e1

VQSLOD
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
SIO_000300: 1.959e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.739e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.451426e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.226e0

QD
type: SiteQuality
SIO_000300: 1.381e1

GenotypeQuality
all individuals: 1051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 281
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52860
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 6614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.451424e6

FS
type: SiteQuality
SIO_000300: 6.946e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 1.484e1

VQSLOD
type: SiteQuality
SIO_000300: -1.972e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.76e0

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

GenotypeQuality
all individuals: 4902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52417
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 19
allele frequency: 1.641043358092935e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 552
allele frequency: 8.27238940175039e-3
allele num: 66728
num of homozygotes: 6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 1.921968095329617e-3
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 35
allele frequency: 2.119670542635659e-3
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 17
allele frequency: 2.57030541276081e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.311258278145695e-3
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.383e1

DP
type: SiteQuality
SIO_000300: 1.545986e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.518e0

FS
type: SiteQuality
SIO_000300: 0.0e0