2-122204900-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204900
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204900
    reference: chr 2
allele count: 1
allele frequency: 2.454590083456063e-5
allele num: 40740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1912+13C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1912+13C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1219+13C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1912+13C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1254+13C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1912+13C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1216+13C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1912+13C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30807
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

2-122204905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204905
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204905
    reference: chr 2
allele count: 1
allele frequency: 2.409870830923462e-5
allele num: 41496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1912+8C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1912+8C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1912+8C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1216+8C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1219+8C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1254+8C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1912+8C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1912+8C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7427
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31424
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1912+8C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

2-122204908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204908
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204908
    reference: chr 2
allele count: 1
allele frequency: 2.399577674329318e-5
allele num: 41674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1912+5C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1912+5C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1254+5C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1219+5C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1216+5C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1912+5C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1912+5C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1912+5C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31407
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1912+5C>T
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

2-122204928-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204928
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204928
    reference: chr 2
allele count: 1
allele frequency: 2.355046865432622e-5
allele num: 42462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1201T>C
  hgvsp: ENSP00000438620.1:p.Ser401Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1897T>C
  hgvsp: ENSP00000389372.2:p.Ser633Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1897T>C
  hgvsp: ENSP00000380717.3:p.Ser633Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1897T>C
  hgvsp: ENSP00000386442.3:p.Ser633Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1897T>C
  hgvsp: ENSP00000263710.4:p.Ser633Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1897T>C
  hgvsp: ENSP00000441625.1:p.Ser633Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1204T>C
  hgvsp: ENSP00000441770.1:p.Ser402Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1239T>C
  hgvsp: ENSP00000400562.2:p.Ser414Pro
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31567
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser633Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

2-122204934-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204934
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204934
    reference: chr 2
allele count: 1
allele frequency: 2.349955350848334e-5
allele num: 42554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1233C>T
  hgvsp: ENSP00000400562.2:p.Pro412Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1891C>T
  hgvsp: ENSP00000263710.4:p.Pro631Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1891C>T
  hgvsp: ENSP00000441625.1:p.Pro631Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1195C>T
  hgvsp: ENSP00000438620.1:p.Pro399Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1198C>T
  hgvsp: ENSP00000441770.1:p.Pro400Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1891C>T
  hgvsp: ENSP00000389372.2:p.Pro631Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1891C>T
  hgvsp: ENSP00000386442.3:p.Pro631Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1891C>T
  hgvsp: ENSP00000380717.3:p.Pro631Ser
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro631Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-122204962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204962
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204962
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 38560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1863G>A
  hgvsp: ENST00000455322.2:c.1863G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1170G>A
  hgvsp: ENST00000541859.1:c.1170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1863G>A
  hgvsp: ENST00000263710.4:c.1863G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1205G>A
  hgvsp: ENST00000452274.2:c.1205G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1863G>A
  hgvsp: ENST00000409078.3:c.1863G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1863G>A
  hgvsp: ENST00000541377.1:c.1863G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1167G>A
  hgvsp: ENST00000545861.1:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1863G>A
  hgvsp: ENST00000397587.3:c.1863G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28889
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr621Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-122204963-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204963
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204963
    reference: chr 2
allele count: 1
allele frequency: 2.58732212160414e-5
allele num: 38650
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1862C>T
  hgvsp: ENSP00000263710.4:p.Thr621Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1862C>T
  hgvsp: ENSP00000386442.3:p.Thr621Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1862C>T
  hgvsp: ENSP00000380717.3:p.Thr621Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1862C>T
  hgvsp: ENSP00000389372.2:p.Thr621Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1169C>T
  hgvsp: ENSP00000441770.1:p.Thr390Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1862C>T
  hgvsp: ENSP00000441625.1:p.Thr621Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1204C>T
  hgvsp: ENSP00000400562.2:p.Thr402Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1166C>T
  hgvsp: ENSP00000438620.1:p.Thr389Met
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28980
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11573
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr621Met
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

2-122204965-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204965
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204965
    reference: chr 2
allele count: 1
allele frequency: 2.614515791675382e-5
allele num: 38248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1860G>C
  hgvsp: ENST00000397587.3:c.1860G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1860G>C
  hgvsp: ENST00000263710.4:c.1860G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1167G>C
  hgvsp: ENST00000541859.1:c.1167G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1860G>C
  hgvsp: ENST00000409078.3:c.1860G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1860G>C
  hgvsp: ENST00000541377.1:c.1860G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1860G>C
  hgvsp: ENST00000455322.2:c.1860G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1164G>C
  hgvsp: ENST00000545861.1:c.1164G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1202G>C
  hgvsp: ENST00000452274.2:c.1202G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12071
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr620Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

2-122204965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204965
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204965
    reference: chr 2
allele count: 1
allele frequency: 2.614515791675382e-5
allele num: 38248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1202G>A
  hgvsp: ENST00000452274.2:c.1202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1860G>A
  hgvsp: ENST00000409078.3:c.1860G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1860G>A
  hgvsp: ENST00000455322.2:c.1860G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1167G>A
  hgvsp: ENST00000541859.1:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1164G>A
  hgvsp: ENST00000545861.1:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1860G>A
  hgvsp: ENST00000397587.3:c.1860G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1860G>A
  hgvsp: ENST00000541377.1:c.1860G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1860G>A
  hgvsp: ENST00000263710.4:c.1860G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12071
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr620Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

2-122204966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204966
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204966
    reference: chr 2
allele count: 1
allele frequency: 2.631440450502605e-5
allele num: 38002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1859C>T
  hgvsp: ENSP00000441625.1:p.Thr620Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1163C>T
  hgvsp: ENSP00000438620.1:p.Thr388Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1859C>T
  hgvsp: ENSP00000380717.3:p.Thr620Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1859C>T
  hgvsp: ENSP00000389372.2:p.Thr620Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1201C>T
  hgvsp: ENSP00000400562.2:p.Thr401Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1166C>T
  hgvsp: ENSP00000441770.1:p.Thr389Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1859C>T
  hgvsp: ENSP00000386442.3:p.Thr620Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1859C>T
  hgvsp: ENSP00000263710.4:p.Thr620Met
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28464
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr620Met
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

2-122204971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204971
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204971
    reference: chr 2
allele count: 1
allele frequency: 2.71370420624152e-5
allele num: 36850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1854G>A
  hgvsp: ENST00000397587.3:c.1854G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1196G>A
  hgvsp: ENST00000452274.2:c.1196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1854G>A
  hgvsp: ENST00000263710.4:c.1854G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1854G>A
  hgvsp: ENST00000541377.1:c.1854G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1854G>A
  hgvsp: ENST00000455322.2:c.1854G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1854G>A
  hgvsp: ENST00000409078.3:c.1854G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1161G>A
  hgvsp: ENST00000541859.1:c.1161G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1158G>A
  hgvsp: ENST00000545861.1:c.1158G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27599
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13585
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser618Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

2-122204972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204972
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204972
    reference: chr 2
allele count: 6
allele frequency: 1.649892756970797e-4
allele num: 36366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1853C>T
  hgvsp: ENSP00000386442.3:p.Ser618Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1853C>T
  hgvsp: ENSP00000263710.4:p.Ser618Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1195C>T
  hgvsp: ENSP00000400562.2:p.Ser399Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1853C>T
  hgvsp: ENSP00000380717.3:p.Ser618Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1160C>T
  hgvsp: ENSP00000441770.1:p.Ser387Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1157C>T
  hgvsp: ENSP00000438620.1:p.Ser386Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1853C>T
  hgvsp: ENSP00000441625.1:p.Ser618Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1853C>T
  hgvsp: ENSP00000389372.2:p.Ser618Leu
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13992
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14057
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser618Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-122204976-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204976
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204976
    reference: chr 2
allele count: 100
allele frequency: 2.767476614822605e-3
allele num: 36134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1153T>C
  hgvsp: ENSP00000438620.1:p.Ser385Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1156T>C
  hgvsp: ENSP00000441770.1:p.Ser386Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1191T>C
  hgvsp: ENSP00000400562.2:p.Ser398Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1849T>C
  hgvsp: ENSP00000263710.4:p.Ser617Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1849T>C
  hgvsp: ENSP00000380717.3:p.Ser617Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1849T>C
  hgvsp: ENSP00000441625.1:p.Ser617Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1849T>C
  hgvsp: ENSP00000389372.2:p.Ser617Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1849T>C
  hgvsp: ENSP00000386442.3:p.Ser617Pro
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 27002
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14642
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 1
hgvs: p.Ser617Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

2-122204983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204983
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204983
    reference: chr 2
allele count: 4
allele frequency: 1.152937107280798e-4
allele num: 34694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1149C>T
  hgvsp: ENST00000541859.1:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1842C>T
  hgvsp: ENST00000541377.1:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1842C>T
  hgvsp: ENST00000397587.3:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1842C>T
  hgvsp: ENST00000409078.3:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1842C>T
  hgvsp: ENST00000263710.4:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1146C>T
  hgvsp: ENST00000545861.1:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1842C>T
  hgvsp: ENST00000455322.2:c.1842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1184C>T
  hgvsp: ENST00000452274.2:c.1184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25555
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16666
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val614Val
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

2-122204993-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122204993
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122204993
    reference: chr 2
allele count: 1
allele frequency: 3.067861087249969e-5
allele num: 32596
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1832A>T
  hgvsp: ENSP00000263710.4:p.Lys611Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1832A>T
  hgvsp: ENSP00000380717.3:p.Lys611Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1832A>T
  hgvsp: ENSP00000389372.2:p.Lys611Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1832A>T
  hgvsp: ENSP00000386442.3:p.Lys611Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1136A>T
  hgvsp: ENSP00000438620.1:p.Lys379Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1139A>T
  hgvsp: ENSP00000441770.1:p.Lys380Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1174A>T
  hgvsp: ENSP00000400562.2:p.Lys392Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1832A>T
  hgvsp: ENSP00000441625.1:p.Lys611Ile
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20016
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19971
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys611Ile
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-122205007-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205007
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205007
    reference: chr 2
allele count: 1
allele frequency: 3.510989396812022e-5
allele num: 28482
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1818A>C
  hgvsp: ENST00000263710.4:c.1818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1125A>C
  hgvsp: ENST00000541859.1:c.1125A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1818A>C
  hgvsp: ENST00000409078.3:c.1818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1818A>C
  hgvsp: ENST00000455322.2:c.1818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1818A>C
  hgvsp: ENST00000541377.1:c.1818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1160A>C
  hgvsp: ENST00000452274.2:c.1160A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1122A>C
  hgvsp: ENST00000545861.1:c.1122A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1818A>C
  hgvsp: ENST00000397587.3:c.1818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24001
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala606Ala
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/2-122205009-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205009
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205009
    reference: chr 2
allele count: 1
allele frequency: 3.542832849146177e-5
allele num: 28226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1123G>T
  hgvsp: ENSP00000441770.1:p.Ala375Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1816G>T
  hgvsp: ENSP00000441625.1:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1816G>T
  hgvsp: ENSP00000380717.3:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1816G>T
  hgvsp: ENSP00000386442.3:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1158G>T
  hgvsp: ENSP00000400562.2:p.Ala387Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1816G>T
  hgvsp: ENSP00000263710.4:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1816G>T
  hgvsp: ENSP00000389372.2:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1120G>T
  hgvsp: ENSP00000438620.1:p.Ala374Ser
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala606Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

2-122205010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205010
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205010
    reference: chr 2
allele count: 14
allele frequency: 4.996431120628123e-4
allele num: 28020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1815C>T
  hgvsp: ENST00000409078.3:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1119C>T
  hgvsp: ENST00000545861.1:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1122C>T
  hgvsp: ENST00000541859.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1815C>T
  hgvsp: ENST00000541377.1:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1815C>T
  hgvsp: ENST00000455322.2:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1815C>T
  hgvsp: ENST00000263710.4:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1815C>T
  hgvsp: ENST00000397587.3:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1157C>T
  hgvsp: ENST00000452274.2:c.1157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19163
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25005
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn605Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

2-122205016-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205016
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205016
    reference: chr 2
allele count: 1
allele frequency: 3.628973726230222e-5
allele num: 27556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1151T>C
  hgvsp: ENST00000452274.2:c.1151T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1809T>C
  hgvsp: ENST00000263710.4:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1113T>C
  hgvsp: ENST00000545861.1:c.1113T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1809T>C
  hgvsp: ENST00000409078.3:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1116T>C
  hgvsp: ENST00000541859.1:c.1116T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1809T>C
  hgvsp: ENST00000397587.3:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1809T>C
  hgvsp: ENST00000455322.2:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1809T>C
  hgvsp: ENST00000541377.1:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7564
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp603Asp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

2-122205029-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205029
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205029
    reference: chr 2
allele count: 2
allele frequency: 7.823501799405414e-5
allele num: 25564
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1796G>A
  hgvsp: ENSP00000263710.4:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1796G>A
  hgvsp: ENSP00000389372.2:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1796G>A
  hgvsp: ENSP00000386442.3:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1138G>A
  hgvsp: ENSP00000400562.2:p.Arg380Gln
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1100G>A
  hgvsp: ENSP00000438620.1:p.Arg367Gln
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1103G>A
  hgvsp: ENSP00000441770.1:p.Arg368Gln
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1796G>A
  hgvsp: ENSP00000441625.1:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1796G>A
  hgvsp: ENSP00000380717.3:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg599Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

2-122205060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205060
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205060
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 23334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1765G>A
  hgvsp: ENSP00000441625.1:p.Val589Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1765G>A
  hgvsp: ENSP00000389372.2:p.Val589Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1107G>A
  hgvsp: ENSP00000400562.2:p.Val370Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1765G>A
  hgvsp: ENSP00000386442.3:p.Val589Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1765G>A
  hgvsp: ENSP00000380717.3:p.Val589Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1765G>A
  hgvsp: ENSP00000263710.4:p.Val589Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1072G>A
  hgvsp: ENSP00000441770.1:p.Val358Met
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1069G>A
  hgvsp: ENSP00000438620.1:p.Val357Met
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 33066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val589Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

2-122205063-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205063
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205063
    reference: chr 2
allele count: 1
allele frequency: 4.309230371455658e-5
allele num: 23206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1762T>C
  hgvsp: ENSP00000389372.2:p.Ser588Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1762T>C
  hgvsp: ENSP00000263710.4:p.Ser588Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1104T>C
  hgvsp: ENSP00000400562.2:p.Ser369Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1069T>C
  hgvsp: ENSP00000441770.1:p.Ser357Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1762T>C
  hgvsp: ENSP00000386442.3:p.Ser588Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1066T>C
  hgvsp: ENSP00000438620.1:p.Ser356Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1762T>C
  hgvsp: ENSP00000441625.1:p.Ser588Pro
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1762T>C
  hgvsp: ENSP00000380717.3:p.Ser588Pro
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6579
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser588Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

2-122205071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205071
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205071
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 22846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1754G>A
  hgvsp: ENSP00000380717.3:p.Ser585Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1058G>A
  hgvsp: ENSP00000438620.1:p.Ser353Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1061G>A
  hgvsp: ENSP00000441770.1:p.Ser354Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1096G>A
  hgvsp: ENSP00000400562.2:p.Ser366Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1754G>A
  hgvsp: ENSP00000386442.3:p.Ser585Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1754G>A
  hgvsp: ENSP00000263710.4:p.Ser585Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1754G>A
  hgvsp: ENSP00000441625.1:p.Ser585Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1754G>A
  hgvsp: ENSP00000389372.2:p.Ser585Asn
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6672
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6636
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31917
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser585Asn
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-122205075-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205075
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205075
    reference: chr 2
allele count: 1
allele frequency: 4.423604352826683e-5
allele num: 22606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1750G>A
  hgvsp: ENSP00000380717.3:p.Val584Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1054G>A
  hgvsp: ENSP00000438620.1:p.Val352Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1057G>A
  hgvsp: ENSP00000441770.1:p.Val353Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1092G>A
  hgvsp: ENSP00000400562.2:p.Val365Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1750G>A
  hgvsp: ENSP00000263710.4:p.Val584Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1750G>A
  hgvsp: ENSP00000386442.3:p.Val584Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1750G>A
  hgvsp: ENSP00000389372.2:p.Val584Ile
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1750G>A
  hgvsp: ENSP00000441625.1:p.Val584Ile
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32978
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31529
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val584Ile
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-122205078-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205078
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205078
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 22308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1089A>G
  hgvsp: ENSP00000400562.2:p.Thr364Ala
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1747A>G
  hgvsp: ENSP00000386442.3:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1054A>G
  hgvsp: ENSP00000441770.1:p.Thr352Ala
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1747A>G
  hgvsp: ENSP00000380717.3:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1747A>G
  hgvsp: ENSP00000263710.4:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1051A>G
  hgvsp: ENSP00000438620.1:p.Thr351Ala
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1747A>G
  hgvsp: ENSP00000389372.2:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1747A>G
  hgvsp: ENSP00000441625.1:p.Thr583Ala
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4572
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30843
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr583Ala
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

2-122205087-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205087
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205087
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 21850
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1742-4A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1742-4A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1049-4A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1742-4A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1084-4A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1046-4A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1742-4A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1742-4A>G
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30218
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1742-4A>G
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

2-122205094-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205094
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205094
    reference: chr 2
allele count: 2
allele frequency: 9.388789784996713e-5
allele num: 21302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1742-11T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1049-11T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1742-11T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1742-11T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1742-11T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1084-11T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1742-11T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1046-11T>C
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30817
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4839
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

2-122205110-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205110
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205110
    reference: chr 2
allele count: 1
allele frequency: 4.921259842519685e-5
allele num: 20320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1046-27T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1084-27T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1742-27T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1742-27T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1049-27T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1742-27T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1742-27T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1742-27T>C
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

2-122205122-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205122
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205122
    reference: chr 2
allele count: 23
allele frequency: 1.193441261934413e-3
allele num: 19272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1084-39A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1742-39A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1742-39A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1049-39A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1742-39A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1742-39A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1046-39A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1742-39A>G
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25683
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-122205125-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205125
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205125
    reference: chr 2
allele count: 1
allele frequency: 5.319148936170213e-5
allele num: 18800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1742-42T>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1742-42T>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1046-42T>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1742-42T>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1084-42T>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1742-42T>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1742-42T>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1049-42T>G
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9793
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-122205128-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205128
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205128
    reference: chr 2
allele count: 1
allele frequency: 5.335609860207022e-5
allele num: 18742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1742-45A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1742-45A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1742-45A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1742-45A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1049-45A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1084-45A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1742-45A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1046-45A>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9894
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15706
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2657
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-122205806-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205806
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205806
    reference: chr 2
allele count: 3
allele frequency: 2.488139866635703e-5
allele num: 120572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+46G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+46G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+46G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+46G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+46G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+46G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+46G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+46G>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2820
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4537
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

2-122205810-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205810
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205810
    reference: chr 2
allele count: 52
allele frequency: 4.311416963767515e-4
allele num: 120610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+42G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+42G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+42G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+42G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+42G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+42G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+42G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+42G>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8390
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10469
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23818
  bin: 9.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

2-122205813-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205813
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205813
    reference: chr 2
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+39C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+39C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+39C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+39C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+39C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+39C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+39C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+39C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-122205816-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205816
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205816
    reference: chr 2
allele count: 3
allele frequency: 2.486902314477087e-5
allele num: 120632
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+36G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+36G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+36G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+36G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+36G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+36G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+36G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+36G>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23776
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

2-122205817-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205817
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205817
    reference: chr 2
allele count: 2
allele frequency: 1.657742486282181e-5
allele num: 120646
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+35C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+35C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+35C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+35C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+35C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+35C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+35C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+35C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-122205823-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205823
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205823
    reference: chr 2
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+29G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+29G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+29G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+29G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+29G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+29G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+29G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+29G>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

2-122205827-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205827
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205827
    reference: chr 2
allele count: 1
allele frequency: 8.287888080359362e-6
allele num: 120658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+25G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+25G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+25G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+25G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+25G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+25G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+25G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+25G>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10566
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4532
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ

2-122205828-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205828
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205828
    reference: chr 2
allele count: 1
allele frequency: 8.287888080359362e-6
allele num: 120658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+24G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+24G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+24G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+24G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+24G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+24G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+24G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+24G>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6362
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4533
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

2-122205833-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205833
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205833
    reference: chr 2
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+19G>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+19G>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+19G>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+19G>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+19G>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+19G>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+19G>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+19G>C
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11462
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6368
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

2-122205837-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205837
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205837
    reference: chr 2
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+15C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+15C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+15C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+15C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+15C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+15C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+15C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+15C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4532
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2299
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

2-122205845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205845
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205845
    reference: chr 2
allele count: 2
allele frequency: 1.657138122462507e-5
allele num: 120690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+7C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+7C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+7C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+7C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+7C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+7C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+7C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+7C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4531
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11564
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1741+7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

2-122205849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205849
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205849
    reference: chr 2
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1045+3G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1741+3G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1741+3G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1741+3G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1741+3G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1048+3G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1741+3G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1083+3G>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4117
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1741+3G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

2-122205867-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205867
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205867
    reference: chr 2
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1726A>C
  hgvsp: ENSP00000389372.2:p.Ser576Arg
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1726A>C
  hgvsp: ENSP00000263710.4:p.Ser576Arg
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1726A>C
  hgvsp: ENSP00000380717.3:p.Ser576Arg
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1033A>C
  hgvsp: ENSP00000441770.1:p.Ser345Arg
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1726A>C
  hgvsp: ENSP00000386442.3:p.Ser576Arg
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1726A>C
  hgvsp: ENSP00000441625.1:p.Ser576Arg
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1030A>C
  hgvsp: ENSP00000438620.1:p.Ser344Arg
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1068A>C
  hgvsp: ENSP00000400562.2:p.Ser357Arg
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11587
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser576Arg
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

2-122205883-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205883
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205883
    reference: chr 2
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1710A>T
  hgvsp: ENSP00000389372.2:p.Lys570Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1710A>T
  hgvsp: ENSP00000263710.4:p.Lys570Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1017A>T
  hgvsp: ENSP00000441770.1:p.Lys339Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1710A>T
  hgvsp: ENSP00000386442.3:p.Lys570Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1014A>T
  hgvsp: ENSP00000438620.1:p.Lys338Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1052A>T
  hgvsp: ENSP00000400562.2:p.Lys351Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1710A>T
  hgvsp: ENSP00000441625.1:p.Lys570Asn
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1710A>T
  hgvsp: ENSP00000380717.3:p.Lys570Asn
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11600
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys570Asn
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-122205892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205892
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205892
    reference: chr 2
allele count: 4
allele frequency: 3.314935441632274e-5
allele num: 120666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1701G>A
  hgvsp: ENST00000409078.3:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1701G>A
  hgvsp: ENST00000263710.4:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1701G>A
  hgvsp: ENST00000397587.3:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1008G>A
  hgvsp: ENST00000541859.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1043G>A
  hgvsp: ENST00000452274.2:c.1043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1701G>A
  hgvsp: ENST00000541377.1:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1005G>A
  hgvsp: ENST00000545861.1:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1701G>A
  hgvsp: ENST00000455322.2:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23772
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu567Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-122205895-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205895
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205895
    reference: chr 2
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1040G>T
  hgvsp: ENST00000452274.2:c.1040G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1698G>T
  hgvsp: ENST00000541377.1:c.1698G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1698G>T
  hgvsp: ENST00000397587.3:c.1698G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1005G>T
  hgvsp: ENST00000541859.1:c.1005G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1698G>T
  hgvsp: ENST00000263710.4:c.1698G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1698G>T
  hgvsp: ENST00000409078.3:c.1698G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1698G>T
  hgvsp: ENST00000455322.2:c.1698G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1002G>T
  hgvsp: ENST00000545861.1:c.1002G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4117
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro566Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

2-122205895-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205895
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205895
    reference: chr 2
allele count: 3
allele frequency: 2.486531288852051e-5
allele num: 120650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1040G>A
  hgvsp: ENST00000452274.2:c.1040G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1698G>A
  hgvsp: ENST00000409078.3:c.1698G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1005G>A
  hgvsp: ENST00000541859.1:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1698G>A
  hgvsp: ENST00000263710.4:c.1698G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1698G>A
  hgvsp: ENST00000541377.1:c.1698G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1698G>A
  hgvsp: ENST00000455322.2:c.1698G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1002G>A
  hgvsp: ENST00000545861.1:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1698G>A
  hgvsp: ENST00000397587.3:c.1698G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6350
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23769
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 11558
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro566Pro
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

2-122205896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205896
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205896
    reference: chr 2
allele count: 3
allele frequency: 2.486613729423271e-5
allele num: 120646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1697C>T
  hgvsp: ENSP00000441625.1:p.Pro566Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1039C>T
  hgvsp: ENSP00000400562.2:p.Pro347Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1697C>T
  hgvsp: ENSP00000386442.3:p.Pro566Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1697C>T
  hgvsp: ENSP00000263710.4:p.Pro566Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1004C>T
  hgvsp: ENSP00000441770.1:p.Pro335Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1697C>T
  hgvsp: ENSP00000380717.3:p.Pro566Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1697C>T
  hgvsp: ENSP00000389372.2:p.Pro566Leu
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.1001C>T
  hgvsp: ENSP00000438620.1:p.Pro334Leu
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4521
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro566Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-122205899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205899
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205899
    reference: chr 2
allele count: 4
allele frequency: 3.315869752636116e-5
allele num: 120632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1036G>A
  hgvsp: ENSP00000400562.2:p.Arg346His
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1694G>A
  hgvsp: ENSP00000386442.3:p.Arg565His
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1694G>A
  hgvsp: ENSP00000441625.1:p.Arg565His
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.998G>A
  hgvsp: ENSP00000438620.1:p.Arg333His
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.1001G>A
  hgvsp: ENSP00000441770.1:p.Arg334His
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1694G>A
  hgvsp: ENSP00000380717.3:p.Arg565His
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1694G>A
  hgvsp: ENSP00000389372.2:p.Arg565His
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1694G>A
  hgvsp: ENSP00000263710.4:p.Arg565His
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg565His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-122205905-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205905
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205905
    reference: chr 2
allele count: 1
allele frequency: 8.29242404139578e-6
allele num: 120592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-4T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-4T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-4T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-4T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-4T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-4T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-4T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-4T>C
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1692-4T>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

2-122205915-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205915
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205915
    reference: chr 2
allele count: 4
allele frequency: 3.319171534784917e-5
allele num: 120512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-14A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-14A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-14A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-14A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-14A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-14A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-14A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-14A>G
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4517
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

2-122205917-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205917
    reference: chr 2
allele count: 1
allele frequency: 8.298892927683448e-6
allele num: 120498
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-16A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-16A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-16A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-16A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-16A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-16A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-16A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-16A>G
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2820
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

2-122205918-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205918
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205918
    reference: chr 2
allele count: 1
allele frequency: 8.298892927683448e-6
allele num: 120498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-17T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-17T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-17T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-17T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-17T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-17T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-17T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-17T>C
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6278
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

2-122205919-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205919
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205919
    reference: chr 2
allele count: 2
allele frequency: 1.659943893896386e-5
allele num: 120486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-18A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-18A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-18A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-18A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-18A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-18A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-18A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-18A>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-122205919-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205919
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205919
    reference: chr 2
allele count: 4
allele frequency: 3.319887787792772e-5
allele num: 120486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-18A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-18A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-18A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-18A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-18A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-18A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-18A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-18A>G
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11079
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4753
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

2-122205921-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205921
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205921
    reference: chr 2
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-20A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-20A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-20A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-20A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-20A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-20A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-20A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-20A>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4753
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

2-122205931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205931
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205931
    reference: chr 2
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-30G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-30G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-30G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-30G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-30G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-30G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-30G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-30G>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4506
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

2-122205933-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205933
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205933
    reference: chr 2
allele count: 3
allele frequency: 2.491239142349405e-5
allele num: 120422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-32A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-32A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-32A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-32A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-32A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-32A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-32A>G
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-32A>G
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10360
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4503
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

2-122205933-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205933
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205933
    reference: chr 2
allele count: 1
allele frequency: 8.304130474498016e-6
allele num: 120422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-32A>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-32A>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-32A>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-32A>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-32A>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-32A>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-32A>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-32A>C
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4503
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4732
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

2-122205935-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205935
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205935
    reference: chr 2
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-34A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-34A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-34A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-34A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-34A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-34A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-34A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-34A>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2793
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23750
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4728
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6129
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

2-122205936-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205936
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205936
    reference: chr 2
allele count: 1
allele frequency: 8.305096006909839e-6
allele num: 120408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-35T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-35T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-35T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-35T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-35T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-35T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-35T>C
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-35T>C
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9783
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4726
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-122205943-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122205943
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122205943
    reference: chr 2
allele count: 1
allele frequency: 8.309788931361144e-6
allele num: 120340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1692-42G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1692-42G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.999-42G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1692-42G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.996-42G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1034-42G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1692-42G>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1692-42G>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8658
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

2-122206494-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206494
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206494
    reference: chr 2
allele count: 9
allele frequency: 8.576656247617595e-5
allele num: 104936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.998+35G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1691+35G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1691+35G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1691+35G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1691+35G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1691+35G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.995+35G>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1033+35G>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15415
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20437
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6719
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD

2-122206501-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206501
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206501
    reference: chr 2
allele count: 2
allele frequency: 1.878392847080038e-5
allele num: 106474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.995+28C>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1033+28C>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1691+28C>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1691+28C>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.998+28C>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1691+28C>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1691+28C>A
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1691+28C>A
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2621
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4928
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29911
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

2-122206505-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206505
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206505
    reference: chr 2
allele count: 1
allele frequency: 9.304575990472114e-6
allele num: 107474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.995+24C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1033+24C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1691+24C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1691+24C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.998+24C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1691+24C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1691+24C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1691+24C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum

2-122206518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206518
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206518
    reference: chr 2
allele count: 6
allele frequency: 5.37952552584862e-5
allele num: 111534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1033+11C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1691+11C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.995+11C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.998+11C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1691+11C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1691+11C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1691+11C>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1691+11C>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36284
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

2-122206520-ATC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206520
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206518
    reference: chr 2
allele count: 2
allele frequency: 1.783071518998627e-5
allele num: 112166
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1691+7_1691+8delGA
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1691+7_1691+8delGA
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.998+7_998+8delGA
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1691+7_1691+8delGA
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1691+7_1691+8delGA
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1691+7_1691+8delGA
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.995+7_995+8delGA
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1033+7_1033+8delGA
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36913
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1691+7_1691+8delGA
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: ATC
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-122206521-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206521
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206521
    reference: chr 2
allele count: 2
allele frequency: 1.779739446145084e-5
allele num: 112376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.998+8A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1691+8A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1033+8A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1691+8A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1691+8A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1691+8A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1691+8A>T
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.995+8A>T
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40397
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1691+8A>T
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

2-122206529-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206529
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206529
    reference: chr 2
allele count: 1
allele frequency: 8.743704532736431e-6
allele num: 114368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1691A>G
  hgvsp: ENSP00000389372.2:p.Asn564Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1691A>G
  hgvsp: ENSP00000380717.3:p.Asn564Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.998A>G
  hgvsp: ENSP00000441770.1:p.Asn333Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1691A>G
  hgvsp: ENSP00000263710.4:p.Asn564Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1033A>G
  hgvsp: ENSP00000400562.2:p.Asn345Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.995A>G
  hgvsp: ENSP00000438620.1:p.Asn332Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1691A>G
  hgvsp: ENSP00000386442.3:p.Asn564Ser
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1691A>G
  hgvsp: ENSP00000441625.1:p.Asn564Ser
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn564Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

2-122206558-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 122206558
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 122206558
    reference: chr 2
allele count: 1
allele frequency: 8.453514125822104e-6
allele num: 118294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441625
  ensembl transcript: ENST00000541377
  gene symbol: CLASP1
  hgvsc: ENST00000541377.1:c.1662C>T
  hgvsp: ENST00000541377.1:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000386442
  ensembl transcript: ENST00000409078
  gene symbol: CLASP1
  hgvsc: ENST00000409078.3:c.1662C>T
  hgvsp: ENST00000409078.3:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000380717
  ensembl transcript: ENST00000397587
  gene symbol: CLASP1
  hgvsc: ENST00000397587.3:c.1662C>T
  hgvsp: ENST00000397587.3:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000441770
  ensembl transcript: ENST00000541859
  gene symbol: CLASP1
  hgvsc: ENST00000541859.1:c.969C>T
  hgvsp: ENST00000541859.1:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000263710
  ensembl transcript: ENST00000263710
  gene symbol: CLASP1
  hgvsc: ENST00000263710.4:c.1662C>T
  hgvsp: ENST00000263710.4:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000438620
  ensembl transcript: ENST00000545861
  gene symbol: CLASP1
  hgvsc: ENST00000545861.1:c.966C>T
  hgvsp: ENST00000545861.1:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000389372
  ensembl transcript: ENST00000455322
  gene symbol: CLASP1
  hgvsc: ENST00000455322.2:c.1662C>T
  hgvsp: ENST00000455322.2:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000074054
  ensembl protein: ENSP00000400562
  ensembl transcript: ENST00000452274
  gene symbol: CLASP1
  hgvsc: ENST00000452274.2:c.1004C>T
  hgvsp: ENST00000452274.2:c.1004C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17088
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg554Arg
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1703
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7880
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2234
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.193317422434368e-4
allele num: 8380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4054
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21842
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.434e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.63e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.26343e5

QD
type: SiteQuality
SIO_000300: 2.28e1

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9988
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2312
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.180469715698393e-4
allele num: 1618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.225e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.38007e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

MQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

QD
type: SiteQuality
SIO_000300: 7.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.424e0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1681
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1360
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.431906614785992e-4
allele num: 4112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

DP
type: SiteQuality
SIO_000300: 7.42409e5

FS
type: SiteQuality
SIO_000300: 1.909e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.629999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

GenotypeQuality
all individuals: 365
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7046
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31649
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10526
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22660
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.440214738897023e-4
allele num: 4098
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.631e0

DP
type: SiteQuality
SIO_000300: 7.55543e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.695e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.59e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.851e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7275
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1278
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 167
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10638
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.416570974295557e-5
allele num: 22642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2436
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.091e-1

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.53384e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.59e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.77e-1

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 338
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11544
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28477
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.0282e5

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

QD
type: SiteQuality
SIO_000300: 9.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.36e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

GenotypeQuality
all individuals: 1194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29068
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8937
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1488
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3776
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20176
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.278e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.34e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.067e0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

DP
type: SiteQuality
SIO_000300: 7.02636e5

GenotypeQuality
all individuals: 1359
bin: 9.75e1
variant carriers: 1

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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.016051364365971e-5
allele num: 19936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1996
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1452
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.073e0

VQSLOD
type: SiteQuality
SIO_000300: -1.907e0

QD
type: SiteQuality
SIO_000300: 6.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.909e0

MQRankSum
type: SiteQuality
SIO_000300: -5.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 6.98199e5

GenotypeQuality
all individuals: 2384
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 195
bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8863
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19936
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.09e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.907e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 6.98199e5

QD
type: SiteQuality
SIO_000300: 6.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 2.909e0

MQRankSum
type: SiteQuality
SIO_000300: -5.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.073e0

GenotypeQuality
all individuals: 1187
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
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variant carriers: 0

GenotypeQuality
all individuals: 28280
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variant carriers: 0

GenotypeQuality
all individuals: 687
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12350
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GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1984
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.676659528907923e-4
allele num: 3736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19766
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.98e-1

QD
type: SiteQuality
SIO_000300: 8.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 6.95471e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.45e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 844
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26860
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 853
bin: 2.75e1
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GenotypeQuality
all individuals: 1355
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1569
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variant carriers: 0

GenotypeQuality
all individuals: 8630
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.236698785085882e-5
allele num: 19096
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-2

DP
type: SiteQuality
SIO_000300: 6.8366e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 2.431e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.74e-2

GenotypeQuality
all individuals: 861
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8538
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variant carriers: 0

GenotypeQuality
all individuals: 25992
bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 240
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variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 8.75e1
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GenotypeQuality
all individuals: 570
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variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 9.75e1
variant carriers: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.596084273249628e-4
allele num: 18796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3598
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.542749173358526e-4
allele num: 8468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1296
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 6.78735e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.84e-2

QD
type: SiteQuality
SIO_000300: 1.211e1

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 8515
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14679
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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 4

GenotypeQuality
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bin: 9.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2676
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 9.75e1
variant carriers: 99

GenotypeQuality
all individuals: 360
bin: 7.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 1.880305146663801e-3
allele num: 18614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2090
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 1.418439716312057e-3
allele num: 8460
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 5.847953216374269e-3
allele num: 342
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 7.82472613458529e-4
allele num: 1278
num of homozygotes: 0

East Asian
type: Population
allele count: 48
allele frequency: 2.696629213483146e-2
allele num: 1780
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 5.602240896358543e-4
allele num: 3570
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

DP
type: SiteQuality
SIO_000300: 6.75019e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.262e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 1527
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 711
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 352
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GenotypeQuality
all individuals: 2272
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variant carriers: 1

GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 326
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GenotypeQuality
all individuals: 488
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GenotypeQuality
all individuals: 1348
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8390
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.772130756382725e-4
allele num: 8382
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.159e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.21e-2

FS
type: SiteQuality
SIO_000300: 3.684e0

VQSLOD
type: SiteQuality
SIO_000300: 2.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

DP
type: SiteQuality
SIO_000300: 6.54296e5

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

GenotypeQuality
all individuals: 20915
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1844
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 411
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 913
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.080505898090721e-5
allele num: 16446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.488e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 6.23749e5

VQSLOD
type: SiteQuality
SIO_000300: -1.221e0

FS
type: SiteQuality
SIO_000300: 5.347e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.79e-2

QD
type: SiteQuality
SIO_000300: 8.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2840
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.424501424501425e-3
allele num: 702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.544e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

FS
type: SiteQuality
SIO_000300: 1.753e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.74e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 5.77397e5

GenotypeQuality
all individuals: 249
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7568
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 9.596928982725527e-4
allele num: 1042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13764
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.881e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 5.75384e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

VQSLOD
type: SiteQuality
SIO_000300: -2.714e0

QD
type: SiteQuality
SIO_000300: 3.49e0

GenotypeQuality
all individuals: 7552
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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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bin: 9.75e1
variant carriers: 16

GenotypeQuality
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GenotypeQuality
all individuals: 1850
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1053
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1020
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.733531451213472e-3
allele num: 8076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.368e0

QD
type: SiteQuality
SIO_000300: 9.58e0

DP
type: SiteQuality
SIO_000300: 5.73506e5

FS
type: SiteQuality
SIO_000300: 3.341e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.758e-1

GenotypeQuality
all individuals: 15157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1038
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GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.51089079164789e-5
allele num: 13314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-1

QD
type: SiteQuality
SIO_000300: 1.082e1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

DP
type: SiteQuality
SIO_000300: 5.614e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

GenotypeQuality
all individuals: 310
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1337
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.330556481172943e-5
allele num: 12004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.254705144291092e-4
allele num: 7970
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

QD
type: SiteQuality
SIO_000300: 1.438e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 1.757e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: -6.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

DP
type: SiteQuality
SIO_000300: 5.23478e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-2

GenotypeQuality
all individuals: 1010
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6917
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2372
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.619999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

VQSLOD
type: SiteQuality
SIO_000300: -1.569e-1

FS
type: SiteQuality
SIO_000300: 2.363e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 9.32e0

DP
type: SiteQuality
SIO_000300: 4.69853e5

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.843e1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.127e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-2

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.632e0

DP
type: SiteQuality
SIO_000300: 4.63643e5

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.09e0

FS
type: SiteQuality
SIO_000300: 4.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.52303e5

QD
type: SiteQuality
SIO_000300: 1.148e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.850000000000001e-2

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

GenotypeQuality
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bin: 9.75e1
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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bin: 7.75e1
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GenotypeQuality
all individuals: 646
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.916699722332408e-5
allele num: 10084
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele 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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.97e-2

FS
type: SiteQuality
SIO_000300: 2.378e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
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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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.31616e5

BaseQRankSum
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.531e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.140000000000001e-2

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

South Asian
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allele frequency: 0.0e0
allele num: 7470
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 1054
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2300
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 3.274e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.190000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.679999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

QD
type: SiteQuality
SIO_000300: 1.444e1

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 990
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

South Asian
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allele frequency: 2.754820936639118e-4
allele num: 7260
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2272
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.33e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.744e0

DP
type: SiteQuality
SIO_000300: 3.92773e5

MQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

QD
type: SiteQuality
SIO_000300: 1.592e1

FS
type: SiteQuality
SIO_000300: 1.485e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-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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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 2234
num of homozygotes: 0

South Asian
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allele frequency: 1.446340757882557e-4
allele num: 6914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.43769e5

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 21

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.148633126579371e-4
allele num: 8706
num of homozygotes: 0

South Asian
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allele count: 22
allele frequency: 3.427859146151449e-3
allele num: 6418
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 2202
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 2202
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 1.661129568106312e-3
allele num: 602
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Latino
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allele num: 390
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 698
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QD
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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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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variant carriers: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.168224299065421e-4
allele num: 8560
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Latino
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Other
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QD
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InbreedingCoeff
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VQSLOD
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DP
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MQ
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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African
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BaseQRankSum
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DP
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QD
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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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Other
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 51
allele frequency: 5.203019791879209e-3
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.37e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.331e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

DP
type: SiteQuality
SIO_000300: 2.519446e6

VQSLOD
type: SiteQuality
SIO_000300: 5.62e0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2297
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4781
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
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: 9806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.426e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.519945e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.204e0

QD
type: SiteQuality
SIO_000300: 1.348e1

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.019783805833163e-4
allele num: 9806
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

DP
type: SiteQuality
SIO_000300: 2.521401e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

QD
type: SiteQuality
SIO_000300: 1.112e1

VQSLOD
type: SiteQuality
SIO_000300: 7.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.217e0

FS
type: SiteQuality
SIO_000300: 2.185e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

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

GenotypeQuality
all individuals: 4118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
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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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 4531
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.019783805833163e-4
allele num: 9806
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: 16504
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.91e-1

DP
type: SiteQuality
SIO_000300: 2.52195e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.99e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 6356
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 72
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GenotypeQuality
all individuals: 2845
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variant carriers: 0

GenotypeQuality
all individuals: 4530
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 23773
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
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: 9806
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: -7.601e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 3.432e0

QD
type: SiteQuality
SIO_000300: 7.11e0

DP
type: SiteQuality
SIO_000300: 2.523402e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.49e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11376
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 6362
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4119
bin: 9.25e1
variant carriers: 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: 9804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.324e0

DP
type: SiteQuality
SIO_000300: 2.524317e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.656e0

QD
type: SiteQuality
SIO_000300: 1.07e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.087e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 23771
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 34
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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
all individuals: 11
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 11414
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
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

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

DP
type: SiteQuality
SIO_000300: 2.524379e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.06e-1

QD
type: SiteQuality
SIO_000300: 1.066e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.44e-1

FS
type: SiteQuality
SIO_000300: 2.226e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
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: -1.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.185e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.525091e6

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 6
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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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GenotypeQuality
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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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 2.525405e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQ
type: SiteQuality
SIO_000300: 5.886e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.027e-1

QD
type: SiteQuality
SIO_000300: 1.115e1

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: 23771
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
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: 16508
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

DP
type: SiteQuality
SIO_000300: 2.525918e6

FS
type: SiteQuality
SIO_000300: 5.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.029e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.264e1

VQSLOD
type: SiteQuality
SIO_000300: -2.307e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2300
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23771
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
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: 66706
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: -3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

DP
type: SiteQuality
SIO_000300: 2.525912e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.289e1

VQSLOD
type: SiteQuality
SIO_000300: 8.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.287e0

GenotypeQuality
all individuals: 2842
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
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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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4778
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.902e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

DP
type: SiteQuality
SIO_000300: 2.526005e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.880000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.28e-1

FS
type: SiteQuality
SIO_000300: 6.854e0

MQRankSum
type: SiteQuality
SIO_000300: -1.314e0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23769
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2841
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 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: 8596
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.39e-1

DP
type: SiteQuality
SIO_000300: 2.525901e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.218e0

MQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.853e0

QD
type: SiteQuality
SIO_000300: 1.155e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.508e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4773
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6353
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 66710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.927e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 4.68e-1

DP
type: SiteQuality
SIO_000300: 2.525242e6

MQRankSum
type: SiteQuality
SIO_000300: -6.98e-1

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2840
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6350
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
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: 1.23e1

FS
type: SiteQuality
SIO_000300: 1.181e0

DP
type: SiteQuality
SIO_000300: 2.525074e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4521
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 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: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49734656552634e-5
allele num: 66706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 1.181e0

DP
type: SiteQuality
SIO_000300: 2.525074e6

QD
type: SiteQuality
SIO_000300: 1.23e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 9.25e1
variant carriers: 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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.524843e6

FS
type: SiteQuality
SIO_000300: 7.773e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.08e-2

GenotypeQuality
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bin: 3.75e1
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: 7.25e1
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
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GenotypeQuality
all individuals: 22
bin: 2.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23763
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.997361161089121e-5
allele num: 66696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 6610
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: -1.138e0

FS
type: SiteQuality
SIO_000300: 1.235e0

DP
type: SiteQuality
SIO_000300: 2.524339e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
all individuals: 4119
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GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 4764
bin: 7.75e1
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GenotypeQuality
all individuals: 23759
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2292
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.783e1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

FS
type: SiteQuality
SIO_000300: 4.336e0

VQSLOD
type: SiteQuality
SIO_000300: -1.678e0

DP
type: SiteQuality
SIO_000300: 2.52311e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.1e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.002581109877247e-5
allele num: 66638
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.338e1

DP
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SIO_000300: 2.519445e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

FS
type: SiteQuality
SIO_000300: 4.748e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.155e0

GenotypeQuality
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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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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

DP
type: SiteQuality
SIO_000300: 2.518338e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

QD
type: SiteQuality
SIO_000300: 1.482e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

VQSLOD
type: SiteQuality
SIO_000300: -1.622e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.170138076293003e-4
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 8.045e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

VQSLOD
type: SiteQuality
SIO_000300: -1.957e-1

QD
type: SiteQuality
SIO_000300: 1.788e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.518183e6

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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bin: 9.75e1
variant carriers: 2

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: 9762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732201628269531e-4
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.06e-1

DP
type: SiteQuality
SIO_000300: 2.51746e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

QD
type: SiteQuality
SIO_000300: 1.587e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

GenotypeQuality
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bin: 8.25e1
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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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001831116981359e-5
allele num: 66626
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732201628269531e-4
allele num: 11546
num of homozygotes: 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: 16506
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
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MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

InbreedingCoeff
type: SiteQuality
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FS
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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
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Other
type: Population
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South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
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MQRankSum
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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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

East Asian
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9760
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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Other
type: Population
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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VQSLOD
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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European (Finnish)
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European (Non-Finnish)
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allele frequency: 4.505316273202379e-5
allele num: 66588
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Latino
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East Asian
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Other
type: Population
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African
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South Asian
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MQ
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SIO_000300: 5.971e1

BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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QD
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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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South Asian
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allele num: 16500
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Other
type: Population
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African
type: Population
allele count: 0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 2.334e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

DP
type: SiteQuality
SIO_000300: 2.507918e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.14e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.262e1

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

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.66e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

FS
type: SiteQuality
SIO_000300: 1.605e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.63e-1

QD
type: SiteQuality
SIO_000300: 1.627e1

DP
type: SiteQuality
SIO_000300: 2.505177e6

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6068
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variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 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: 16496
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.502232e6

MQRankSum
type: SiteQuality
SIO_000300: 9.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

QD
type: SiteQuality
SIO_000300: 1.425e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

GenotypeQuality
all individuals: 23741
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
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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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 4476
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.490751e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

VQSLOD
type: SiteQuality
SIO_000300: -2.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.468e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.353e0

QD
type: SiteQuality
SIO_000300: 4.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 6071
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2704
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variant carriers: 9

GenotypeQuality
all individuals: 21694
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 1.031991744066047e-4
allele num: 9690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.625087891998312e-4
allele num: 14222
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.119e0

DP
type: SiteQuality
SIO_000300: 1.185922e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

QD
type: SiteQuality
SIO_000300: 1.102e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

GenotypeQuality
all individuals: 587
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 2970
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variant carriers: 0

GenotypeQuality
all individuals: 1169
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 230
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variant carriers: 0

GenotypeQuality
all individuals: 891
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 397
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 405
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variant carriers: 0

GenotypeQuality
all individuals: 595
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.907985631389887e-5
allele num: 14476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.696410395602904e-5
allele num: 58948
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.755e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.262151e6

VQSLOD
type: SiteQuality
SIO_000300: -2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.876e0

QD
type: SiteQuality
SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 600
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2644
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.838074398249453e-5
allele num: 14624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.029999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.857e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.293151e6

MQ
type: SiteQuality
SIO_000300: 5.863e1

FS
type: SiteQuality
SIO_000300: 0.0e0

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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variant carriers: 6

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: 3128
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.121579183490354e-4
allele num: 8916
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.079632861482774e-5
allele num: 61884
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15166
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

FS
type: SiteQuality
SIO_000300: 7.802e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.493e0

DP
type: SiteQuality
SIO_000300: 1.38423e6

QD
type: SiteQuality
SIO_000300: 1.065e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1758
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

GenotypeQuality
all individuals: 462
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10438
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.233139794551139e-4
allele num: 8956
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15248
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.373e1

FS
type: SiteQuality
SIO_000300: 9.659000000000001e0

DP
type: SiteQuality
SIO_000300: 1.392477e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 639
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GenotypeQuality
all individuals: 2698
bin: 9.75e1
variant carriers: 2

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15262
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.472799208704253e-4
allele num: 8088
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.024e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.494e1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 1.396246e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

GenotypeQuality
all individuals: 561
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43442
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3402
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.456611570247934e-5
allele num: 15488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.42e0

DP
type: SiteQuality
SIO_000300: 1.430415e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1