3-33592806-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592806
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592806
    reference: chr 3
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3115C>T
  hgvsp: ENSP00000419974.2:p.Arg1039Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2422C>T
  hgvsp: ENSP00000439039.1:p.Arg808Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3088C>T
  hgvsp: ENSP00000352581.5:p.Arg1030Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1558C>T
  hgvsp: ENSP00000304743.7:p.Arg520Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3112C>T
  hgvsp: ENSP00000382297.4:p.Arg1038Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2452C>T
  hgvsp: ENSP00000417518.1:p.Arg818Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.281C>T
  hgvsp: ENSP00000417386.1:p.Arg95Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2392C>T
  hgvsp: ENSP00000419305.3:p.Arg798Cys
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3599
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9729
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg1039Cys
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

3-33592834-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592834
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592834
    reference: chr 3
allele count: 7
allele frequency: 5.798830293089451e-5
allele num: 120714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.253A>G
  hgvsp: ENST00000480385.1:c.253A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3060A>G
  hgvsp: ENST00000359576.5:c.3060A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2424A>G
  hgvsp: ENST00000480013.1:c.2424A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3087A>G
  hgvsp: ENST00000468888.2:c.3087A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3084A>G
  hgvsp: ENST00000399362.4:c.3084A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2394A>G
  hgvsp: ENST00000539981.1:c.2394A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1530A>G
  hgvsp: ENST00000307312.7:c.1530A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2364A>G
  hgvsp: ENST00000461133.3:c.2364A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro1029Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

3-33592863-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592863
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592863
    reference: chr 3
allele count: 6
allele frequency: 4.973392350922564e-5
allele num: 120642
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2335A>G
  hgvsp: ENSP00000419305.3:p.Ile779Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3055A>G
  hgvsp: ENSP00000382297.4:p.Ile1019Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1501A>G
  hgvsp: ENSP00000304743.7:p.Ile501Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3058A>G
  hgvsp: ENSP00000419974.2:p.Ile1020Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2395A>G
  hgvsp: ENSP00000417518.1:p.Ile799Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3031A>G
  hgvsp: ENSP00000352581.5:p.Ile1011Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2365A>G
  hgvsp: ENSP00000439039.1:p.Ile789Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.224A>G
  hgvsp: ENSP00000417386.1:p.Ile76Val
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9212
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9719
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile1020Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

3-33592877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592877
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592877
    reference: chr 3
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2381C>T
  hgvsp: ENSP00000417518.1:p.Ala794Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3044C>T
  hgvsp: ENSP00000419974.2:p.Ala1015Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1487C>T
  hgvsp: ENSP00000304743.7:p.Ala496Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2351C>T
  hgvsp: ENSP00000439039.1:p.Ala784Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3041C>T
  hgvsp: ENSP00000382297.4:p.Ala1014Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2321C>T
  hgvsp: ENSP00000419305.3:p.Ala774Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3017C>T
  hgvsp: ENSP00000352581.5:p.Ala1006Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.210C>T
  hgvsp: ENSP00000417386.1:p.Ala71Val
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25469
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala1015Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

3-33592907-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592907
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592907
    reference: chr 3
allele count: 2
allele frequency: 1.666666666666667e-5
allele num: 120000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2341-20C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2371-20C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2311-20C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1477-20C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3031-20C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.200-20C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3007-20C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3034-20C>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12063
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9688
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23160
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-33592913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592913
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592913
    reference: chr 3
allele count: 1
allele frequency: 8.339170752860335e-6
allele num: 119916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3031-26C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2311-26C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2341-26C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2371-26C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1477-26C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.200-26C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3007-26C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3034-26C>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

3-33592913-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592913
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592913
    reference: chr 3
allele count: 355
allele frequency: 2.960405617265419e-3
allele num: 119916
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.200-26C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2311-26C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1477-26C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2371-26C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3034-26C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3007-26C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3031-26C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2341-26C>G
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16063
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 3.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 3.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 4.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 8182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 5
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

3-33592914-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592914
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592914
    reference: chr 3
allele count: 3
allele frequency: 2.502794787512722e-5
allele num: 119866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2371-27C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3007-27C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3031-27C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3034-27C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1477-27C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2341-27C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2311-27C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.200-27C>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6965
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3438
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

3-33592917-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592917
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592917
    reference: chr 3
allele count: 1
allele frequency: 8.343763037129745e-6
allele num: 119850
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3034-30T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3031-30T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2341-30T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3007-30T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.200-30T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2371-30T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1477-30T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2311-30T>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21612
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

3-33592927-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592927
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592927
    reference: chr 3
allele count: 8
allele frequency: 6.689075068144953e-5
allele num: 119598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3007-40A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.200-40A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2341-40A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2311-40A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2371-40A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3034-40A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3031-40A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1477-40A>G
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13179
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2593
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17057
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-33592932-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33592932
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33592932
    reference: chr 3
allele count: 1
allele frequency: 8.379981899239097e-6
allele num: 119332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3007-45C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1477-45C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3034-45C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.200-45C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2371-45C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2311-45C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2341-45C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3031-45C>G
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11437
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/3-33600567-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600567
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600567
    reference: chr 3
allele count: 1
allele frequency: 8.450228156160216e-5
allele num: 11834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+232G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+232G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.199+50G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+232G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.136G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+232G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+232G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+232G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+232G>T
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

3-33600567-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600567
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600565
    reference: chr 3
allele count: 1
allele frequency: 8.450228156160216e-5
allele num: 11834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.199+48_199+49delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+230_3006+231delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+230_2370+231delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+230_2310+231delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+230_1476+231delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.134_135delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+230_2340+231delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+230_3030+231delCT
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+230_3033+231delCT
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1869
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: CAG
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/3-33600582-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600582
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600582
    reference: chr 3
allele count: 425
allele frequency: 3.48132372214941e-2
allele num: 12208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+217T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.121T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+217T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+217T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.199+35T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+217T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+217T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+217T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+217T>G
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.5e0
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 2.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 2.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 3.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 7
num of homozygotes: 8
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/3-33600586-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600586
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600586
    reference: chr 3
allele count: 24
allele frequency: 1.949317738791423e-3
allele num: 12312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+213T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+213T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.117T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+213T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+213T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+213T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+213T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+213T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.199+31T>G
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

3-33600590-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600590
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600590
    reference: chr 3
allele count: 26
allele frequency: 2.094409537618817e-3
allele num: 12414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+209A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+209A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+209A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+209A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.199+27A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.113A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+209A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+209A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+209A>C
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

3-33600633-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600633
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600633
    reference: chr 3
allele count: 1
allele frequency: 7.106310403638431e-5
allele num: 14072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+166C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+166C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+166C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+166C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.183C>G
  hgvsp: ENSP00000417386.1:p.Ser62Cys
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+166C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+166C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+166C>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.70C>G
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser62Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

3-33600661-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600661
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600661
    reference: chr 3
allele count: 2
allele frequency: 1.302592158395207e-4
allele num: 15354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+138A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.155A>C
  hgvsp: ENSP00000417386.1:p.Lys53Gln
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+138A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+138A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.42A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+138A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+138A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+138A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+138A>C
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9237
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys53Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

3-33600665-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600665
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600665
    reference: chr 3
allele count: 1
allele frequency: 6.365372374283896e-5
allele num: 15710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+134A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+134A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+134A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+134A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+134A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.151A>T
  hgvsp: ENST00000480385.1:c.151A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.38A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+134A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+134A>T
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10049
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4958
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
hgvs: c.151A>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

3-33600667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600667
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600667
    reference: chr 3
allele count: 1
allele frequency: 6.310740880979428e-5
allele num: 15846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+132A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+132A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+132A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+132A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.149A>G
  hgvsp: ENSP00000417386.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+132A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+132A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+132A>G
  variant of: http://identifiers.org/hgnc/17078
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr51Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

3-33600694-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600694
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600694
    reference: chr 3
allele count: 3
allele frequency: 1.712524260760361e-4
allele num: 17518
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+105G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.36-27G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+105G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+105G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+105G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+105G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.149-27G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+105G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+105G>A
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19980
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17992
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

3-33600695-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600695
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600695
    reference: chr 3
allele count: 118
allele frequency: 6.684037611872663e-3
allele num: 17654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+104A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+104A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+104A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.36-28A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+104A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+104A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.149-28A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+104A>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+104A>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 20533
  bin: 2.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18537
  bin: 7.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 4
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

3-33600751-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600751
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600751
    reference: chr 3
allele count: 1
allele frequency: 3.766478342749529e-5
allele num: 26550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.148+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.35+48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+48T>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3730
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7931
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7479
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7437
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

3-33600758-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600758
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600758
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 26788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.35+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+41A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.148+41A>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19792
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

3-33600774-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600774
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600774
    reference: chr 3
allele count: 2
allele frequency: 6.87426960885406e-5
allele num: 29094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.148+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.35+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+25A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+25A>G
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28069
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

3-33600782-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600782
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600782
    reference: chr 3
allele count: 1
allele frequency: 3.109066036562616e-5
allele num: 32164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.35+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+17T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.148+17T>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9710
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-33600786-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600786
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600786
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 34272
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.35+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+13G>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.148+13G>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34789
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8043
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/3-33600789-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600789
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600789
    reference: chr 3
allele count: 1
allele frequency: 2.773771219349828e-5
allele num: 36052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2370+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.148+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3006+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1476+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2340+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2310+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3030+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3033+10T>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.35+10T>G
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6570
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-33600803-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600803
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600803
    reference: chr 3
allele count: 1
allele frequency: 2.283313544615947e-5
allele num: 43796
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.3002T>C
  hgvsp: ENSP00000352581.5:p.Leu1001Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2336T>C
  hgvsp: ENSP00000439039.1:p.Leu779Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2366T>C
  hgvsp: ENSP00000417518.1:p.Leu789Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3029T>C
  hgvsp: ENSP00000419974.2:p.Leu1010Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3026T>C
  hgvsp: ENSP00000382297.4:p.Leu1009Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2306T>C
  hgvsp: ENSP00000419305.3:p.Leu769Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1472T>C
  hgvsp: ENSP00000304743.7:p.Leu491Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.31T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.144T>C
  hgvsp: ENSP00000417386.1:p.Leu49Ser
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34337
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3612
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu1010Ser
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

3-33600806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600806
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600806
    reference: chr 3
allele count: 1
allele frequency: 2.18789655625082e-5
allele num: 45706
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3026G>A
  hgvsp: ENSP00000419974.2:p.Ser1009Asn
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1469G>A
  hgvsp: ENSP00000304743.7:p.Ser490Asn
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2999G>A
  hgvsp: ENSP00000352581.5:p.Ser1000Asn
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.28G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2333G>A
  hgvsp: ENSP00000439039.1:p.Ser778Asn
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2363G>A
  hgvsp: ENSP00000417518.1:p.Ser788Asn
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3023G>A
  hgvsp: ENSP00000382297.4:p.Ser1008Asn
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2303G>A
  hgvsp: ENSP00000419305.3:p.Ser768Asn
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.141G>A
  hgvsp: ENSP00000417386.1:p.Ser48Asn
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser1009Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

3-33600815-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600815
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600815
    reference: chr 3
allele count: 1
allele frequency: 2.028891413731537e-5
allele num: 49288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2990A>G
  hgvsp: ENSP00000352581.5:p.Gln997Arg
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3017A>G
  hgvsp: ENSP00000419974.2:p.Gln1006Arg
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.19A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3014A>G
  hgvsp: ENSP00000382297.4:p.Gln1005Arg
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.132A>G
  hgvsp: ENSP00000417386.1:p.Gln45Arg
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1460A>G
  hgvsp: ENSP00000304743.7:p.Gln487Arg
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2294A>G
  hgvsp: ENSP00000419305.3:p.Gln765Arg
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2354A>G
  hgvsp: ENSP00000417518.1:p.Gln785Arg
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2324A>G
  hgvsp: ENSP00000439039.1:p.Gln775Arg
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln1006Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

3-33600829-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600829
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600829
    reference: chr 3
allele count: 1
allele frequency: 1.916222741731499e-5
allele num: 52186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2280A>G
  hgvsp: ENST00000461133.3:c.2280A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1446A>G
  hgvsp: ENST00000307312.7:c.1446A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.3000A>G
  hgvsp: ENST00000399362.4:c.3000A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2976A>G
  hgvsp: ENST00000359576.5:c.2976A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.3003A>G
  hgvsp: ENST00000468888.2:c.3003A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000163539
  ensembl transcript: ENST00000493577
  gene symbol: CLASP2
  hgvsc: ENST00000493577.1:n.5A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2340A>G
  hgvsp: ENST00000480013.1:c.2340A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2310A>G
  hgvsp: ENST00000539981.1:c.2310A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.118A>G
  hgvsp: ENST00000480385.1:c.118A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1727
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr1001Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-33600836-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600836
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600836
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 51822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2333G>C
  hgvsp: ENSP00000417518.1:p.Arg778Thr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2273G>C
  hgvsp: ENSP00000419305.3:p.Arg758Thr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2303G>C
  hgvsp: ENSP00000439039.1:p.Arg768Thr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2969G>C
  hgvsp: ENSP00000352581.5:p.Arg990Thr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.111G>C
  hgvsp: ENSP00000417386.1:p.Arg38Thr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2996G>C
  hgvsp: ENSP00000419974.2:p.Arg999Thr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1439G>C
  hgvsp: ENSP00000304743.7:p.Arg480Thr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2993G>C
  hgvsp: ENSP00000382297.4:p.Arg998Thr
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31255
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg999Thr
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

3-33600848-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600848
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600848
    reference: chr 3
allele count: 3
allele frequency: 5.941299956430467e-5
allele num: 50494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1427A>G
  hgvsp: ENSP00000304743.7:p.Asn476Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2984A>G
  hgvsp: ENSP00000419974.2:p.Asn995Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2291A>G
  hgvsp: ENSP00000439039.1:p.Asn764Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2981A>G
  hgvsp: ENSP00000382297.4:p.Asn994Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2321A>G
  hgvsp: ENSP00000417518.1:p.Asn774Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2957A>G
  hgvsp: ENSP00000352581.5:p.Asn986Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.99A>G
  hgvsp: ENSP00000417386.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2261A>G
  hgvsp: ENSP00000419305.3:p.Asn754Ser
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31100
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 2.75e1
  variant carriers: 1
hgvs: p.Asn995Ser
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

3-33600850-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600850
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600850
    reference: chr 3
allele count: 4
allele frequency: 7.970350296895549e-5
allele num: 50186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2289C>T
  hgvsp: ENST00000539981.1:c.2289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2979C>T
  hgvsp: ENST00000399362.4:c.2979C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2319C>T
  hgvsp: ENST00000480013.1:c.2319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2955C>T
  hgvsp: ENST00000359576.5:c.2955C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2259C>T
  hgvsp: ENST00000461133.3:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2982C>T
  hgvsp: ENST00000468888.2:c.2982C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1425C>T
  hgvsp: ENST00000307312.7:c.1425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.97C>T
  hgvsp: ENST00000480385.1:c.97C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33387
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11248
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe994Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

3-33600853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600853
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600853
    reference: chr 3
allele count: 1
allele frequency: 2.005454837157067e-5
allele num: 49864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2316G>A
  hgvsp: ENST00000480013.1:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2256G>A
  hgvsp: ENST00000461133.3:c.2256G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1422G>A
  hgvsp: ENST00000307312.7:c.1422G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2979G>A
  hgvsp: ENST00000468888.2:c.2979G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.94G>A
  hgvsp: ENST00000480385.1:c.94G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2952G>A
  hgvsp: ENST00000359576.5:c.2952G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2976G>A
  hgvsp: ENST00000399362.4:c.2976G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2286G>A
  hgvsp: ENST00000539981.1:c.2286G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4360
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln993Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-33600865-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600865
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600865
    reference: chr 3
allele count: 2
allele frequency: 4.202740186601664e-5
allele num: 47588
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2967A>C
  hgvsp: ENST00000468888.2:c.2967A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2304A>C
  hgvsp: ENST00000480013.1:c.2304A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2940A>C
  hgvsp: ENST00000359576.5:c.2940A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1410A>C
  hgvsp: ENST00000307312.7:c.1410A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2244A>C
  hgvsp: ENST00000461133.3:c.2244A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2274A>C
  hgvsp: ENST00000539981.1:c.2274A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.82A>C
  hgvsp: ENST00000480385.1:c.82A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2964A>C
  hgvsp: ENST00000399362.4:c.2964A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29926
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6443
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32860
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro989Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-33600866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600866
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600866
    reference: chr 3
allele count: 1
allele frequency: 2.106504887091338e-5
allele num: 47472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2243C>T
  hgvsp: ENSP00000419305.3:p.Pro748Leu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2963C>T
  hgvsp: ENSP00000382297.4:p.Pro988Leu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1409C>T
  hgvsp: ENSP00000304743.7:p.Pro470Leu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.81C>T
  hgvsp: ENSP00000417386.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2939C>T
  hgvsp: ENSP00000352581.5:p.Pro980Leu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2966C>T
  hgvsp: ENSP00000419974.2:p.Pro989Leu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2303C>T
  hgvsp: ENSP00000417518.1:p.Pro768Leu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2273C>T
  hgvsp: ENSP00000439039.1:p.Pro758Leu
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro989Leu
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: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

3-33600868-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600868
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600868
    reference: chr 3
allele count: 2
allele frequency: 4.228866240960799e-5
allele num: 47294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2241T>C
  hgvsp: ENST00000461133.3:c.2241T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2964T>C
  hgvsp: ENST00000468888.2:c.2964T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2301T>C
  hgvsp: ENST00000480013.1:c.2301T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2937T>C
  hgvsp: ENST00000359576.5:c.2937T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1407T>C
  hgvsp: ENST00000307312.7:c.1407T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.79T>C
  hgvsp: ENST00000480385.1:c.79T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2961T>C
  hgvsp: ENST00000399362.4:c.2961T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2271T>C
  hgvsp: ENST00000539981.1:c.2271T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8321
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8391
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32860
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe988Phe
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS

3-33600871-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600871
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600871
    reference: chr 3
allele count: 1
allele frequency: 2.158615032595087e-5
allele num: 46326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.76T>C
  hgvsp: ENST00000480385.1:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2238T>C
  hgvsp: ENST00000461133.3:c.2238T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2268T>C
  hgvsp: ENST00000539981.1:c.2268T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2934T>C
  hgvsp: ENST00000359576.5:c.2934T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2298T>C
  hgvsp: ENST00000480013.1:c.2298T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2958T>C
  hgvsp: ENST00000399362.4:c.2958T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1404T>C
  hgvsp: ENST00000307312.7:c.1404T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2961T>C
  hgvsp: ENST00000468888.2:c.2961T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7817
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8040
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser987Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-33600880-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600880
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600880
    reference: chr 3
allele count: 1
allele frequency: 2.241549358916883e-5
allele num: 44612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-3C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-3C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-3C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-3C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-3C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-3C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-3C>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-3C>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10050
  bin: 7.5e0
  variant carriers: 0
hgvs: c.2955-3C>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-33600881-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600881
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600881
    reference: chr 3
allele count: 18
allele frequency: 4.084225812307134e-4
allele num: 44072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-4T>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-4T>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-4T>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-4T>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-4T>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-4T>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-4T>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-4T>A
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26978
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8879
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
hgvs: c.2955-4T>A
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-33600900-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600900
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600900
    reference: chr 3
allele count: 1
allele frequency: 2.594302910807866e-5
allele num: 38546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-23G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-23G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-23G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-23G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-23G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-23G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-23G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-23G>A
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23070
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

3-33600906-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600906
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600906
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 36850
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-29T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-29T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-29T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-29T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-29T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-29T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-29T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-29T>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22682
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2158
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-33600912-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600912
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600912
    reference: chr 3
allele count: 1
allele frequency: 2.849002849002849e-5
allele num: 35100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-35A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-35A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-35A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-35A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-35A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-35A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-35A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-35A>G
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6572
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4646
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

3-33600913-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600913
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600913
    reference: chr 3
allele count: 50
allele frequency: 1.433568438557257e-3
allele num: 34878
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-36A>G
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-36A>G
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22153
  bin: 7.5e0
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19171
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 1.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3753
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

3-33600914-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600914
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600914
    reference: chr 3
allele count: 1
allele frequency: 2.93789294318115e-5
allele num: 34038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-37T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-37T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-37T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-37T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-37T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-37T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-37T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-37T>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3438
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21049
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

3-33600917-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600917
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600917
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 33138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-40A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-40A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-40A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-40A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-40A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-40A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-40A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-40A>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22510
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5839
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21126
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3075
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 4.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

3-33600921-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600921
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600921
    reference: chr 3
allele count: 1
allele frequency: 3.121293464011486e-5
allele num: 32038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-44T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-44T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-44T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-44T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-44T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-44T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-44T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-44T>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22878
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10767
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6532
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

3-33600925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600925
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600925
    reference: chr 3
allele count: 3
allele frequency: 9.700575567483671e-5
allele num: 30926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-48T>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-48T>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23087
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19323
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 20144
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6542
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

3-33600926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33600926
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33600926
    reference: chr 3
allele count: 3
allele frequency: 9.786012526096034e-5
allele num: 30656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2292-49G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2955-49G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.70-49G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2928-49G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2262-49G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2952-49G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1398-49G>A
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2232-49G>A
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23062
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7025
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3684
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

3-33602254-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602254
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602254
    reference: chr 3
allele count: 1
allele frequency: 8.47371453750466e-6
allele num: 118012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2291+46G>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2231+46G>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1397+46G>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2927+46G>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.69+46G>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2951+46G>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2954+46G>C
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2261+46G>C
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

3-33602281-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602281
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602281
    reference: chr 3
allele count: 1
allele frequency: 8.395882659143956e-6
allele num: 119106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2927+19A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2231+19A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2954+19A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2951+19A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2291+19A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1397+19A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.69+19A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2261+19A>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37753
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2564
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

3-33602294-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602294
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602294
    reference: chr 3
allele count: 1
allele frequency: 8.330001332800213e-6
allele num: 120048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2261+6A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2291+6A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2951+6A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2231+6A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1397+6A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2927+6A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.69+6A>T
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2954+6A>T
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
hgvs: c.2954+6A>T
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

3-33602308-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602308
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602308
    reference: chr 3
allele count: 3
allele frequency: 2.486737400530504e-5
allele num: 120640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2223T>C
  hgvsp: ENST00000461133.3:c.2223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.61T>C
  hgvsp: ENST00000480385.1:c.61T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2283T>C
  hgvsp: ENST00000480013.1:c.2283T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2919T>C
  hgvsp: ENST00000359576.5:c.2919T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2253T>C
  hgvsp: ENST00000539981.1:c.2253T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1389T>C
  hgvsp: ENST00000307312.7:c.1389T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2946T>C
  hgvsp: ENST00000468888.2:c.2946T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2943T>C
  hgvsp: ENST00000399362.4:c.2943T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp982Asp
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

3-33602314-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602314
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602314
    reference: chr 3
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.55C>G
  hgvsp: ENST00000480385.1:c.55C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2247C>G
  hgvsp: ENST00000539981.1:c.2247C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1383C>G
  hgvsp: ENST00000307312.7:c.1383C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2913C>G
  hgvsp: ENST00000359576.5:c.2913C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2277C>G
  hgvsp: ENST00000480013.1:c.2277C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2940C>G
  hgvsp: ENST00000468888.2:c.2940C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2217C>G
  hgvsp: ENST00000461133.3:c.2217C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2937C>G
  hgvsp: ENST00000399362.4:c.2937C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala980Ala
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: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

3-33602337-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602337
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602337
    reference: chr 3
allele count: 6
allele frequency: 4.968944099378882e-5
allele num: 120750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1360G>A
  hgvsp: ENSP00000304743.7:p.Val454Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2914G>A
  hgvsp: ENSP00000382297.4:p.Val972Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2917G>A
  hgvsp: ENSP00000419974.2:p.Val973Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2224G>A
  hgvsp: ENSP00000439039.1:p.Val742Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2254G>A
  hgvsp: ENSP00000417518.1:p.Val752Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.32G>A
  hgvsp: ENSP00000417386.1:p.Val12Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2194G>A
  hgvsp: ENSP00000419305.3:p.Val732Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2890G>A
  hgvsp: ENSP00000352581.5:p.Val964Ile
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9438
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val973Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

3-33602341-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602341
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602341
    reference: chr 3
allele count: 2
allele frequency: 1.656232402530723e-5
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2913A>G
  hgvsp: ENST00000468888.2:c.2913A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1356A>G
  hgvsp: ENST00000307312.7:c.1356A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2886A>G
  hgvsp: ENST00000359576.5:c.2886A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2190A>G
  hgvsp: ENST00000461133.3:c.2190A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.28A>G
  hgvsp: ENST00000480385.1:c.28A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2250A>G
  hgvsp: ENST00000480013.1:c.2250A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2220A>G
  hgvsp: ENST00000539981.1:c.2220A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2910A>G
  hgvsp: ENST00000399362.4:c.2910A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26540
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3926
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly971Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

3-33602342-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602342
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602342
    reference: chr 3
allele count: 2
allele frequency: 1.656204971927326e-5
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.27G>C
  hgvsp: ENSP00000417386.1:p.Gly10Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2909G>C
  hgvsp: ENSP00000382297.4:p.Gly970Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2885G>C
  hgvsp: ENSP00000352581.5:p.Gly962Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2249G>C
  hgvsp: ENSP00000417518.1:p.Gly750Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1355G>C
  hgvsp: ENSP00000304743.7:p.Gly452Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2912G>C
  hgvsp: ENSP00000419974.2:p.Gly971Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2219G>C
  hgvsp: ENSP00000439039.1:p.Gly740Ala
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2189G>C
  hgvsp: ENSP00000419305.3:p.Gly730Ala
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3925
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39341
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly971Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

3-33602354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602354
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602354
    reference: chr 3
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1343C>T
  hgvsp: ENSP00000304743.7:p.Ala448Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2900C>T
  hgvsp: ENSP00000419974.2:p.Ala967Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2237C>T
  hgvsp: ENSP00000417518.1:p.Ala746Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.15C>T
  hgvsp: ENSP00000417386.1:p.Ala6Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2207C>T
  hgvsp: ENSP00000439039.1:p.Ala736Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2873C>T
  hgvsp: ENSP00000352581.5:p.Ala958Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2177C>T
  hgvsp: ENSP00000419305.3:p.Ala726Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2897C>T
  hgvsp: ENSP00000382297.4:p.Ala966Val
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala967Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

3-33602360-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602360
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602359
    reference: chr 3
allele count: 2
allele frequency: 1.656314699792961e-5
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2230delA
  hgvsp: ENSP00000417518.1:p.Met744TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2170delA
  hgvsp: ENSP00000419305.3:p.Met724TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2890delA
  hgvsp: ENSP00000382297.4:p.Met964TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2866delA
  hgvsp: ENSP00000352581.5:p.Met956TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417386
  ensembl transcript: ENST00000480385
  gene symbol: CLASP2
  hgvsc: ENST00000480385.1:c.8delA
  hgvsp: ENSP00000417386.1:p.Met4TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2200delA
  hgvsp: ENSP00000439039.1:p.Met734TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2893delA
  hgvsp: ENSP00000419974.2:p.Met965TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1336delA
  hgvsp: ENSP00000304743.7:p.Met446TrpfsTer33
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met965TrpfsTer33
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: AT
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

3-33602385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602385
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602385
    reference: chr 3
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2842C>T
  hgvsp: ENST00000359576.5:c.2842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2866C>T
  hgvsp: ENST00000399362.4:c.2866C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1312C>T
  hgvsp: ENST00000307312.7:c.1312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2869C>T
  hgvsp: ENST00000468888.2:c.2869C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2146C>T
  hgvsp: ENST00000461133.3:c.2146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2206C>T
  hgvsp: ENST00000480013.1:c.2206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2176C>T
  hgvsp: ENST00000539981.1:c.2176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39327
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3921
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu957Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-33602394-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602394
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602394
    reference: chr 3
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2857T>G
  hgvsp: ENSP00000382297.4:p.Leu953Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2167T>G
  hgvsp: ENSP00000439039.1:p.Leu723Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2860T>G
  hgvsp: ENSP00000419974.2:p.Leu954Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2833T>G
  hgvsp: ENSP00000352581.5:p.Leu945Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2137T>G
  hgvsp: ENSP00000419305.3:p.Leu713Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2197T>G
  hgvsp: ENSP00000417518.1:p.Leu733Val
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1303T>G
  hgvsp: ENSP00000304743.7:p.Leu435Val
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu954Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

3-33602401-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602401
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602401
    reference: chr 3
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2190A>G
  hgvsp: ENST00000480013.1:c.2190A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2130A>G
  hgvsp: ENST00000461133.3:c.2130A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1296A>G
  hgvsp: ENST00000307312.7:c.1296A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2850A>G
  hgvsp: ENST00000399362.4:c.2850A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2160A>G
  hgvsp: ENST00000539981.1:c.2160A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2853A>G
  hgvsp: ENST00000468888.2:c.2853A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2826A>G
  hgvsp: ENST00000359576.5:c.2826A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39259
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln951Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

3-33602411-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602411
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602411
    reference: chr 3
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1286A>G
  hgvsp: ENSP00000304743.7:p.Asp429Gly
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2840A>G
  hgvsp: ENSP00000382297.4:p.Asp947Gly
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2180A>G
  hgvsp: ENSP00000417518.1:p.Asp727Gly
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2816A>G
  hgvsp: ENSP00000352581.5:p.Asp939Gly
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2843A>G
  hgvsp: ENSP00000419974.2:p.Asp948Gly
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2120A>G
  hgvsp: ENSP00000419305.3:p.Asp707Gly
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2150A>G
  hgvsp: ENSP00000439039.1:p.Asp717Gly
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39213
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9415
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp948Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/3-33602412-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602412
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602412
    reference: chr 3
allele count: 4
allele frequency: 3.315594900615043e-5
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2815G>T
  hgvsp: ENSP00000352581.5:p.Asp939Tyr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2119G>T
  hgvsp: ENSP00000419305.3:p.Asp707Tyr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1285G>T
  hgvsp: ENSP00000304743.7:p.Asp429Tyr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2149G>T
  hgvsp: ENSP00000439039.1:p.Asp717Tyr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2842G>T
  hgvsp: ENSP00000419974.2:p.Asp948Tyr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2839G>T
  hgvsp: ENSP00000382297.4:p.Asp947Tyr
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2179G>T
  hgvsp: ENSP00000417518.1:p.Asp727Tyr
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39154
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp948Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS

3-33602412-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602412
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602412
    reference: chr 3
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2842G>C
  hgvsp: ENSP00000419974.2:p.Asp948His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2119G>C
  hgvsp: ENSP00000419305.3:p.Asp707His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2815G>C
  hgvsp: ENSP00000352581.5:p.Asp939His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2149G>C
  hgvsp: ENSP00000439039.1:p.Asp717His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2839G>C
  hgvsp: ENSP00000382297.4:p.Asp947His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2179G>C
  hgvsp: ENSP00000417518.1:p.Asp727His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1285G>C
  hgvsp: ENSP00000304743.7:p.Asp429His
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9412
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp948His
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

3-33602421-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602421
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602421
    reference: chr 3
allele count: 1
allele frequency: 8.296414289743973e-6
allele num: 120534
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2140G>A
  hgvsp: ENSP00000439039.1:p.Val714Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2833G>A
  hgvsp: ENSP00000419974.2:p.Val945Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1276G>A
  hgvsp: ENSP00000304743.7:p.Val426Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2830G>A
  hgvsp: ENSP00000382297.4:p.Val944Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2110G>A
  hgvsp: ENSP00000419305.3:p.Val704Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2806G>A
  hgvsp: ENSP00000352581.5:p.Val936Ile
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2170G>A
  hgvsp: ENSP00000417518.1:p.Val724Ile
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39077
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val945Ile
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

3-33602422-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602422
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602422
    reference: chr 3
allele count: 1
allele frequency: 8.298204268596276e-6
allele num: 120508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2139A>T
  hgvsp: ENSP00000439039.1:p.Gln713His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2169A>T
  hgvsp: ENSP00000417518.1:p.Gln723His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2829A>T
  hgvsp: ENSP00000382297.4:p.Gln943His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2832A>T
  hgvsp: ENSP00000419974.2:p.Gln944His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2805A>T
  hgvsp: ENSP00000352581.5:p.Gln935His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1275A>T
  hgvsp: ENSP00000304743.7:p.Gln425His
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2109A>T
  hgvsp: ENSP00000419305.3:p.Gln703His
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2594
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2782
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln944His
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

3-33602422-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602422
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602422
    reference: chr 3
allele count: 3
allele frequency: 2.489461280578883e-5
allele num: 120508
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2139A>G
  hgvsp: ENST00000539981.1:c.2139A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2829A>G
  hgvsp: ENST00000399362.4:c.2829A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2805A>G
  hgvsp: ENST00000359576.5:c.2805A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1275A>G
  hgvsp: ENST00000307312.7:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2109A>G
  hgvsp: ENST00000461133.3:c.2109A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2169A>G
  hgvsp: ENST00000480013.1:c.2169A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2832A>G
  hgvsp: ENST00000468888.2:c.2832A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln944Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

3-33602424-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33602424
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33602424
    reference: chr 3
allele count: 14
allele frequency: 1.16198001394376e-4
allele num: 120484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000439039
  ensembl transcript: ENST00000539981
  gene symbol: CLASP2
  hgvsc: ENST00000539981.1:c.2137C>G
  hgvsp: ENSP00000439039.1:p.Gln713Glu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000304743
  ensembl transcript: ENST00000307312
  gene symbol: CLASP2
  hgvsc: ENST00000307312.7:c.1273C>G
  hgvsp: ENSP00000304743.7:p.Gln425Glu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000382297
  ensembl transcript: ENST00000399362
  gene symbol: CLASP2
  hgvsc: ENST00000399362.4:c.2827C>G
  hgvsp: ENSP00000382297.4:p.Gln943Glu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419974
  ensembl transcript: ENST00000468888
  gene symbol: CLASP2
  hgvsc: ENST00000468888.2:c.2830C>G
  hgvsp: ENSP00000419974.2:p.Gln944Glu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000352581
  ensembl transcript: ENST00000359576
  gene symbol: CLASP2
  hgvsc: ENST00000359576.5:c.2803C>G
  hgvsp: ENSP00000352581.5:p.Gln935Glu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000419305
  ensembl transcript: ENST00000461133
  gene symbol: CLASP2
  hgvsc: ENST00000461133.3:c.2107C>G
  hgvsp: ENSP00000419305.3:p.Gln703Glu
  variant of: http://identifiers.org/hgnc/17078
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163539
  ensembl protein: ENSP00000417518
  ensembl transcript: ENST00000480013
  gene symbol: CLASP2
  hgvsc: ENST00000480013.1:c.2167C>G
  hgvsp: ENSP00000417518.1:p.Gln723Glu
  variant of: http://identifiers.org/hgnc/17078
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14426
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln944Glu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4685
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25981
bin: 6.25e1
variant carriers: 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: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 9802
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: -1.947e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.35e-1

FS
type: SiteQuality
SIO_000300: 1.584e0

MQRankSum
type: SiteQuality
SIO_000300: -1.888e0

DP
type: SiteQuality
SIO_000300: 2.123303e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.85e-1

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9729
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 9252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25903
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4687
bin: 7.75e1
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: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.994693131052679e-5
allele num: 66706
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: 9794
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: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.699e0

DP
type: SiteQuality
SIO_000300: 2.122834e6

FS
type: SiteQuality
SIO_000300: 1.818e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

QD
type: SiteQuality
SIO_000300: 1.262e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25808
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.132461161079313e-4
allele num: 9784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.537e0

DP
type: SiteQuality
SIO_000300: 2.120259e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.95e1

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

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

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9156
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4641
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9711
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
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: 898
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.005e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

DP
type: SiteQuality
SIO_000300: 2.115304e6

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.743e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.896e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3064
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8727
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
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: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014499743767522e-5
allele num: 66346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.144e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 8.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.228e0

DP
type: SiteQuality
SIO_000300: 2.078748e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.45e-1

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9919
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8182
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.67e0

QD
type: SiteQuality
SIO_000300: 1.194e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

DP
type: SiteQuality
SIO_000300: 2.064066e6

GenotypeQuality
all individuals: 244
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9919
bin: 9.75e1
variant carriers: 348

GenotypeQuality
all individuals: 254
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4351
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1820
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3427
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.2271714922049e-3
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 8.000984736582965e-4
allele num: 16248
num of homozygotes: 1

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

Latino
type: Population
allele count: 51
allele frequency: 4.425546685178757e-3
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 270
allele frequency: 4.071661237785016e-3
allele num: 66312
num of homozygotes: 4

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.077155824508321e-4
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.333059885151764e-3
allele num: 9752
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.194e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
type: SiteQuality
SIO_000300: 2.064066e6

FS
type: SiteQuality
SIO_000300: 2.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
all individuals: 1202
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9602
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.525706010137581e-5
allele num: 66288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.956e0

VQSLOD
type: SiteQuality
SIO_000300: -7.173e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

QD
type: SiteQuality
SIO_000300: 5.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 2.578e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 2.058252e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4332
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166588894073728e-4
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66274
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.456e0

VQSLOD
type: SiteQuality
SIO_000300: -8.227e-1

FS
type: SiteQuality
SIO_000300: 3.256e0

DP
type: SiteQuality
SIO_000300: 2.047995e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.117e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.644e0

MQ
type: SiteQuality
SIO_000300: 6.019e1

QD
type: SiteQuality
SIO_000300: 1.306e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 392
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.216926869350862e-4
allele num: 9736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16118
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.007371e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

QD
type: SiteQuality
SIO_000300: 1.51e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

GenotypeQuality
all individuals: 3345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9593
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variant carriers: 1

GenotypeQuality
all individuals: 4131
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.902e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.990261e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

QD
type: SiteQuality
SIO_000300: 1.18e1

GenotypeQuality
all individuals: 97
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 1

GenotypeQuality
all individuals: 777
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3682
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.42571998859424e-4
allele num: 7014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.11e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

DP
type: SiteQuality
SIO_000300: 1.30847e5

QD
type: SiteQuality
SIO_000300: 1.431e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

GenotypeQuality
all individuals: 416
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
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variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 453
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GenotypeQuality
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GenotypeQuality
all individuals: 391
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GenotypeQuality
all individuals: 716
bin: 3.75e1
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GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 780
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GenotypeQuality
all individuals: 63
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variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.42571998859424e-4
allele num: 7014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

QD
type: SiteQuality
SIO_000300: 1.431e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.26e-1

DP
type: SiteQuality
SIO_000300: 1.30847e5

GenotypeQuality
all individuals: 128
bin: 8.25e1
variant carriers: 7

GenotypeQuality
all individuals: 250
bin: 1.25e1
variant carriers: 5

GenotypeQuality
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bin: 6.25e1
variant carriers: 12

GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 218
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variant carriers: 2

GenotypeQuality
all individuals: 221
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variant carriers: 6

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 2

GenotypeQuality
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bin: 9.75e1
variant carriers: 400

GenotypeQuality
all individuals: 483
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GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 11

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 89
allele frequency: 2.352008456659619e-2
allele num: 3784
num of homozygotes: 0

South Asian
type: Population
allele count: 240
allele frequency: 3.311258278145696e-2
allele num: 7248
num of homozygotes: 5

Latino
type: Population
allele count: 8
allele frequency: 4.347826086956522e-2
allele num: 184
num of homozygotes: 0

African
type: Population
allele count: 82
allele frequency: 1.29746835443038e-1
allele num: 632
num of homozygotes: 3

Other
type: Population
allele count: 6
allele frequency: 4.477611940298507e-2
allele num: 134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.461e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.46328e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.91e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 28

GenotypeQuality
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GenotypeQuality
all individuals: 175
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 524
bin: 3.25e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.374003847210772e-4
allele num: 7278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 3.52760736196319e-2
allele num: 652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.50525e5

MQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.38e-2

QD
type: SiteQuality
SIO_000300: 2.009e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 72
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GenotypeQuality
all individuals: 152
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GenotypeQuality
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GenotypeQuality
all individuals: 244
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 106
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variant carriers: 28

GenotypeQuality
all individuals: 58
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.365001365001365e-4
allele num: 7326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3862
num of homozygotes: 0

African
type: Population
allele count: 25
allele frequency: 3.753753753753754e-2
allele num: 666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-2

DP
type: SiteQuality
SIO_000300: 1.56097e5

FS
type: SiteQuality
SIO_000300: 7.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.607e-1

QD
type: SiteQuality
SIO_000300: 1.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

GenotypeQuality
all individuals: 112
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4589
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.287664177182591e-4
allele num: 7766
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4768
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

VQSLOD
type: SiteQuality
SIO_000300: -4.243e0

QD
type: SiteQuality
SIO_000300: 1.655e1

MQRankSum
type: SiteQuality
SIO_000300: -1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.183e0

DP
type: SiteQuality
SIO_000300: 1.93414e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.9e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.552974214960429e-4
allele num: 7834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.72e-2

FS
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-1

DP
type: SiteQuality
SIO_000300: 2.17239e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.171e0

QD
type: SiteQuality
SIO_000300: 1.197e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 8.375209380234506e-4
allele num: 1194
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.85e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

QD
type: SiteQuality
SIO_000300: 7.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.23338e5

GenotypeQuality
all individuals: 94
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variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.684068710003368e-4
allele num: 5938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.905e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.88e-2

FS
type: SiteQuality
SIO_000300: 3.735e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 2.26472e5

VQSLOD
type: SiteQuality
SIO_000300: -3.566e0

QD
type: SiteQuality
SIO_000300: 6.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.587e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 101
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.825554705432288e-4
allele num: 7842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 4.216e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.814e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.99e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.64176e5

QD
type: SiteQuality
SIO_000300: 1.066e1

GenotypeQuality
all individuals: 5285
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 206
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GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 4

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 465
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 210
bin: 9.75e1
variant carriers: 109

GenotypeQuality
all individuals: 1038
bin: 6.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.418037436188315e-4
allele num: 7052
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.08641975308642e-3
allele num: 324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

African
type: Population
allele count: 116
allele frequency: 7.341772151898734e-2
allele num: 1580
num of homozygotes: 4

DP
type: SiteQuality
SIO_000300: 2.68041e5

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

FS
type: SiteQuality
SIO_000300: 1.259e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.370000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.032e0

QD
type: SiteQuality
SIO_000300: 1.371e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12154
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.681885125184094e-4
allele num: 2716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
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VQSLOD
type: SiteQuality
SIO_000300: -1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.45876e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.275e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.18e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.369e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12298
num of homozygotes: 0

Latino
type: Population
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Other
type: Population
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MQRankSum
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.763e1

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6086
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 3.331112591605596e-4
allele num: 3002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1984
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.084598698481562e-3
allele num: 922
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
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BaseQRankSum
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SIO_000300: 1.06e0

FS
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DP
type: SiteQuality
SIO_000300: 7.47213e5

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1114
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1572
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 6.47920176234288e-5
allele num: 15434
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -3.58e-1

DP
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
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SIO_000300: 6.98e-1

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 16616
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 1262
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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SIO_000300: 0.0e0

MQRankSum
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 2080
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1404
num of homozygotes: 0

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

South Asian
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allele frequency: 1.185395922238028e-4
allele num: 8436
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17580
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.3469e5

MQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

FS
type: SiteQuality
SIO_000300: 1.814e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.511e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 1.19e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

VQSLOD
type: SiteQuality
SIO_000300: 4.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8884
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2874
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 3.194888178913738e-4
allele num: 3130
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2022
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 21870
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.069e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

DP
type: SiteQuality
SIO_000300: 9.04584e5

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

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

East Asian
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allele frequency: 0.0e0
allele num: 3382
num of homozygotes: 0

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

Latino
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allele frequency: 4.528985507246377e-4
allele num: 2208
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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Other
type: Population
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MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

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

European (Non-Finnish)
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allele frequency: 3.994886545222116e-5
allele num: 25032
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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South Asian
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European (Finnish)
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Other
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num of homozygotes: 0

African
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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Latino
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African
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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FS
type: SiteQuality
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BaseQRankSum
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QD
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5170
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3236
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.518796992481203e-4
allele num: 2660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25946
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.079447322970639e-4
allele num: 9264
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 9.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

DP
type: SiteQuality
SIO_000300: 9.23355e5

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

QD
type: SiteQuality
SIO_000300: 1.184e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3218
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9244
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 1.550387596899225e-4
allele num: 25800
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

FS
type: SiteQuality
SIO_000300: 2.45e0

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.601e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.19852e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 4.43e0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.90411493714375e-5
allele num: 25614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5092
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3718
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9222
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.134e0

MQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.917e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.157e1

DP
type: SiteQuality
SIO_000300: 9.11846e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 4846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.184100418410042e-4
allele num: 2390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.107788366743346e-5
allele num: 24344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.082e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.96e-1

DP
type: SiteQuality
SIO_000300: 8.70562e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2386
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.06782464846981e-4
allele num: 4836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24270
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.433e0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

VQSLOD
type: SiteQuality
SIO_000300: -8.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

QD
type: SiteQuality
SIO_000300: 8.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-1

DP
type: SiteQuality
SIO_000300: 8.7095e5

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24190
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 6.578947368421052e-4
allele num: 3040
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.63276e5

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.093e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 136
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.235852253473399e-5
allele num: 23608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2278
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9002
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
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QD
type: SiteQuality
SIO_000300: 9.720000000000001e0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -8.413e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 2892
num of homozygotes: 0

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

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

Latino
type: Population
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allele frequency: 4.725897920604915e-4
allele num: 2116
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
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South Asian
type: Population
allele count: 18
allele frequency: 2.029769959404601e-3
allele num: 8868
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.07e-2

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.14592e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

QD
type: SiteQuality
SIO_000300: 1.217e1

GenotypeQuality
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1474
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.497502497502498e-4
allele num: 4004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.14e-2

QD
type: SiteQuality
SIO_000300: 1.395e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.408e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 7.53458e5

GenotypeQuality
all individuals: 3448
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4519
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.221e0

MQ
type: SiteQuality
SIO_000300: 5.616e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.49e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
SIO_000300: -1.803e0

QD
type: SiteQuality
SIO_000300: 4.8e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 7.30607e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeQuality
all individuals: 2876
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20800
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3865
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.203948952564411e-4
allele num: 8306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2072
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.83e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

QD
type: SiteQuality
SIO_000300: 6.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

DP
type: SiteQuality
SIO_000300: 7.08066e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.114e-1

GenotypeQuality
all individuals: 2909
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 15767
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 20878
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 4826
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1540
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 9.75e1
variant carriers: 59

GenotypeQuality
all individuals: 517
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 276
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 748
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1284
bin: 2.75e1
variant carriers: 1

East Asian
type: Population
allele count: 46
allele frequency: 2.237354085603113e-2
allele num: 2056
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1102
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.205690860863275e-4
allele num: 8294
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 5.458515283842794e-4
allele num: 3664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.048780487804878e-3
allele num: 328
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

DP
type: SiteQuality
SIO_000300: 7.04851e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.82e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 1.591e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3489
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14301
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5269
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2314
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.768549280177187e-4
allele num: 3612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1976
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.435e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

DP
type: SiteQuality
SIO_000300: 6.97593e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 9.59e0

GenotypeQuality
all individuals: 3899
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 1086
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

DP
type: SiteQuality
SIO_000300: 6.8859e5

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.459e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 494
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20996
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GenotypeQuality
all individuals: 4793
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
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GenotypeQuality
all individuals: 2313
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2668
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
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variant carriers: 0

GenotypeQuality
all individuals: 356
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variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.495193556767992e-5
allele num: 15396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2248
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.114e0

DP
type: SiteQuality
SIO_000300: 6.80788e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.26e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.114e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 7.49e0

GenotypeQuality
all individuals: 8370
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 3.25e1
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GenotypeQuality
all individuals: 7096
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
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GenotypeQuality
all individuals: 192
bin: 8.75e1
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GenotypeQuality
all individuals: 2313
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 508
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 996
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
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variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.240694789081886e-3
allele num: 806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.785181164337088e-5
allele num: 14738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.097893432465923e-4
allele num: 3228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2206
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.524e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 6.76246e5

GenotypeQuality
all individuals: 510
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1027
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
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variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 5.75e1
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GenotypeQuality
all individuals: 6244
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.363698349924997e-4
allele num: 14666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3222
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.266784899923993e-4
allele num: 7894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1566
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.56e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 6.76277e5

QD
type: SiteQuality
SIO_000300: 1.354e1

GenotypeQuality
all individuals: 1166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3941
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515381118351265e-5
allele num: 65990
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.347e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.585e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e0

QD
type: SiteQuality
SIO_000300: 6.63e0

VQSLOD
type: SiteQuality
SIO_000300: -4.595e0

FS
type: SiteQuality
SIO_000300: 4.559e0

DP
type: SiteQuality
SIO_000300: 1.829785e6

MQ
type: SiteQuality
SIO_000300: 5.884e1

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.506180871828237e-5
allele num: 15370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.0e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 1.862684e6

FS
type: SiteQuality
SIO_000300: 2.752e0

VQSLOD
type: SiteQuality
SIO_000300: -4.659e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.84e-1

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

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 430
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020616452337212e-4
allele num: 9798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16052
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

VQSLOD
type: SiteQuality
SIO_000300: 6.860000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.88e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.12e0

DP
type: SiteQuality
SIO_000300: 1.877001e6

FS
type: SiteQuality
SIO_000300: 6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 9408
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variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.458e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 2.308e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 1.885482e6

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

QD
type: SiteQuality
SIO_000300: 1.216e1

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2779
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.88e1

FS
type: SiteQuality
SIO_000300: 3.696e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.434e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.075e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

DP
type: SiteQuality
SIO_000300: 1.886094e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 6
allele frequency: 6.955715279387897e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.65e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.887369e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.184e0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.673e0

QD
type: SiteQuality
SIO_000300: 1.132e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
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: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e0

QD
type: SiteQuality
SIO_000300: 1.387e1

DP
type: SiteQuality
SIO_000300: 1.886985e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.99e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
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GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.843e0

QD
type: SiteQuality
SIO_000300: 8.880000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

FS
type: SiteQuality
SIO_000300: 5.134e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 1.886713e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3923
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variant carriers: 2

GenotypeQuality
all individuals: 1351
bin: 8.25e1
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: 6614
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.055e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
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SIO_000300: 1.29e0

BaseQRankSum
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SIO_000300: -2.218e0

InbreedingCoeff
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SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.886835e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

South Asian
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allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.74e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
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SIO_000300: -1.63e-1

ClippingRankSum
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SIO_000300: 8.89e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
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VQSLOD
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SIO_000300: 2.18e0

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
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FS
type: SiteQuality
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VQSLOD
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SIO_000300: 3.52e-1

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.886657e6

MQ
type: SiteQuality
SIO_000300: 5.918e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

Latino
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allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.88644e6

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

BaseQRankSum
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SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.516e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 7.87e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -9.2e-1

BaseQRankSum
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SIO_000300: 3.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.885987e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.2e-2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 4
allele frequency: 5.999880002399952e-5
allele num: 66668
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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VQSLOD
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.39e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66590
num of homozygotes: 0

East Asian
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Latino
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African
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ReadPosRankSum
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

African
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Other
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South Asian
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allele num: 16496
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East Asian
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European (Non-Finnish)
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European (Finnish)
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MQ
type: SiteQuality
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ReadPosRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 39034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818622696411251e-4
allele num: 16496
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.491e1

DP
type: SiteQuality
SIO_000300: 1.882189e6