20-20050455-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20050455
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20050455
    reference: chr 20
allele count: 2
allele frequency: 1.637197118533071e-4
allele num: 12216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*42A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.6-1043A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.144-1043A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1789-1043A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.144-1043A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.144-1043A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.144-1043A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.144-1043A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1789-1043A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-20051477-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051477
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051477
    reference: chr 20
allele count: 6
allele frequency: 5.238253217160518e-5
allele num: 114542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1789-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.144-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.144-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.6-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.144-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.144-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1789-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.144-21C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*133-21C>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32060
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4656
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

20-20051479-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051479
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051479
    reference: chr 20
allele count: 1
allele frequency: 8.692326414241508e-6
allele num: 115044
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*133-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.144-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.144-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.6-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.144-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1789-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.144-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.144-19A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1789-19A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

20-20051491-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051491
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051491
    reference: chr 20
allele count: 2
allele frequency: 1.70695070326369e-5
allele num: 117168
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.144-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.144-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1789-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.144-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.144-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.144-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*133-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1789-7T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.6-7T>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7010
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 2.25e1
  variant carriers: 0
hgvs: c.144-7T>C
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

20-20051494-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051494
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051494
    reference: chr 20
allele count: 1
allele frequency: 8.493434575073469e-6
allele num: 117738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.144-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.6-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.144-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.144-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.144-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1789-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1789-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.144-4G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*133-4G>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12300
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
hgvs: c.144-4G>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

20-20051502-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051502
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051502
    reference: chr 20
allele count: 1
allele frequency: 8.391655337931961e-6
allele num: 119166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1785A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.148A>G
  hgvsp: ENSP00000414537.2:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.10A>G
  hgvsp: ENSP00000345553.6:p.Lys4Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.148A>G
  hgvsp: ENSP00000366521.1:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.148A>G
  hgvsp: ENSP00000417086.1:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1785A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.148A>G
  hgvsp: ENSP00000245957.5:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.148A>G
  hgvsp: ENSP00000366518.2:p.Lys50Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*137A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7212
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys50Glu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

20-20051504-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051504
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051504
    reference: chr 20
allele count: 1
allele frequency: 8.378577652657685e-6
allele num: 119352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.150G>A
  hgvsp: ENST00000377306.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.12G>A
  hgvsp: ENST00000340348.6:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1783G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.150G>A
  hgvsp: ENST00000377303.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.150G>A
  hgvsp: ENST00000451767.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*139G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.150G>A
  hgvsp: ENST00000245957.5:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1783G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.150G>A
  hgvsp: ENST00000475466.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys50Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

20-20051505-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051505
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051505
    reference: chr 20
allele count: 1
allele frequency: 8.370021929457456e-6
allele num: 119474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.151G>T
  hgvsp: ENSP00000414537.2:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1782G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*140G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.151G>T
  hgvsp: ENSP00000417086.1:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.151G>T
  hgvsp: ENSP00000245957.5:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.151G>T
  hgvsp: ENSP00000366521.1:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1782G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.151G>T
  hgvsp: ENSP00000366518.2:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.13G>T
  hgvsp: ENSP00000345553.6:p.Ala5Ser
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala51Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

20-20051514-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051514
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051514
    reference: chr 20
allele count: 23
allele frequency: 1.910489417549922e-4
allele num: 120388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.160G>T
  hgvsp: ENSP00000366521.1:p.Ala54Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.160G>T
  hgvsp: ENSP00000417086.1:p.Ala54Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.160G>T
  hgvsp: ENSP00000414537.2:p.Ala54Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.160G>T
  hgvsp: ENSP00000245957.5:p.Ala54Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1773G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1773G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*149G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.22G>T
  hgvsp: ENSP00000345553.6:p.Ala8Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.160G>T
  hgvsp: ENSP00000366518.2:p.Ala54Ser
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala54Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

20-20051519-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051519
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051519
    reference: chr 20
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.27T>C
  hgvsp: ENST00000340348.6:c.27T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.165T>C
  hgvsp: ENST00000377303.2:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1768T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.165T>C
  hgvsp: ENST00000475466.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.165T>C
  hgvsp: ENST00000245957.5:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*154T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.165T>C
  hgvsp: ENST00000451767.2:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.165T>C
  hgvsp: ENST00000377306.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1768T>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val55Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/20-20051525-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051525
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051525
    reference: chr 20
allele count: 629
allele frequency: 5.20230257716611e-3
allele num: 120908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1762C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.171C>A
  hgvsp: ENST00000245957.5:c.171C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1762C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.171C>A
  hgvsp: ENST00000377303.2:c.171C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.171C>A
  hgvsp: ENST00000451767.2:c.171C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.33C>A
  hgvsp: ENST00000340348.6:c.33C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.171C>A
  hgvsp: ENST00000475466.1:c.171C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*160C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.171C>A
  hgvsp: ENST00000377306.1:c.171C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 4.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 34976
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.75e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 13592
  bin: 2.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu57Leu
num of homozygotes: 27
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/20-20051535-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051535
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051535
    reference: chr 20
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.181A>C
  hgvsp: ENSP00000414537.2:p.Lys61Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.43A>C
  hgvsp: ENSP00000345553.6:p.Lys15Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1752A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*170A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.181A>C
  hgvsp: ENSP00000366521.1:p.Lys61Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.181A>C
  hgvsp: ENSP00000245957.5:p.Lys61Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.181A>C
  hgvsp: ENSP00000366518.2:p.Lys61Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.181A>C
  hgvsp: ENSP00000417086.1:p.Lys61Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1752A>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys61Gln
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

20-20051537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051537
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051537
    reference: chr 20
allele count: 2
allele frequency: 1.650573574317075e-5
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.183G>A
  hgvsp: ENST00000451767.2:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.183G>A
  hgvsp: ENST00000377306.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.183G>A
  hgvsp: ENST00000475466.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1750G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.183G>A
  hgvsp: ENST00000245957.5:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.183G>A
  hgvsp: ENST00000377303.2:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1750G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.45G>A
  hgvsp: ENST00000340348.6:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*172G>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys61Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

20-20051539-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051539
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051539
    reference: chr 20
allele count: 2
allele frequency: 1.650382888830209e-5
allele num: 121184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1748A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.185A>G
  hgvsp: ENSP00000366521.1:p.Glu62Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1748A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.185A>G
  hgvsp: ENSP00000417086.1:p.Glu62Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.185A>G
  hgvsp: ENSP00000366518.2:p.Glu62Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.47A>G
  hgvsp: ENSP00000345553.6:p.Glu16Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*174A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.185A>G
  hgvsp: ENSP00000414537.2:p.Glu62Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.185A>G
  hgvsp: ENSP00000245957.5:p.Glu62Gly
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu62Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/20-20051546-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051546
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051546
    reference: chr 20
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.192C>A
  hgvsp: ENST00000451767.2:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1741C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*181C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.54C>A
  hgvsp: ENST00000340348.6:c.54C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.192C>A
  hgvsp: ENST00000475466.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.192C>A
  hgvsp: ENST00000377306.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1741C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.192C>A
  hgvsp: ENST00000245957.5:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.192C>A
  hgvsp: ENST00000377303.2:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4758
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile64Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

20-20051574-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051574
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051574
    reference: chr 20
allele count: 10
allele frequency: 8.243615319934711e-5
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.220C>T
  hgvsp: ENSP00000366521.1:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.220C>T
  hgvsp: ENSP00000414537.2:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1713C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.82C>T
  hgvsp: ENSP00000345553.6:p.Pro28Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*209C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.220C>T
  hgvsp: ENSP00000245957.5:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.220C>T
  hgvsp: ENSP00000366518.2:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.220C>T
  hgvsp: ENSP00000417086.1:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1713C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14143
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro74Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

20-20051607-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051607
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051608
    reference: chr 20
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.254dupT
  hgvsp: ENSP00000245957.5:p.Ser86ValfsTer9
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.254dupT
  hgvsp: ENSP00000366518.2:p.Ser86ValfsTer9
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1679dupT
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1679dupT
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.254dupT
  hgvsp: ENSP00000366521.1:p.Ser86ValfsTer9
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*243dupT
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.116dupT
  hgvsp: ENSP00000345553.6:p.Ser40ValfsTer9
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.254dupT
  hgvsp: ENSP00000417086.1:p.Ser86ValfsTer9
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.254dupT
  hgvsp: ENSP00000414537.2:p.Ser86ValfsTer9
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37396
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser86ValfsTer9
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

20-20051619-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051619
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051619
    reference: chr 20
allele count: 4
allele frequency: 3.302400845414616e-5
allele num: 121124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.265C>G
  hgvsp: ENSP00000414537.2:p.Arg89Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1668C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.265C>G
  hgvsp: ENSP00000366518.2:p.Arg89Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.265C>G
  hgvsp: ENSP00000245957.5:p.Arg89Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.265C>G
  hgvsp: ENSP00000417086.1:p.Arg89Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*254C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.265C>G
  hgvsp: ENSP00000366521.1:p.Arg89Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.127C>G
  hgvsp: ENSP00000345553.6:p.Arg43Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1668C>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg89Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

20-20051619-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051619
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051619
    reference: chr 20
allele count: 5
allele frequency: 4.128001056768271e-5
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1668C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.265C>T
  hgvsp: ENSP00000417086.1:p.Arg89Trp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*254C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.265C>T
  hgvsp: ENSP00000366518.2:p.Arg89Trp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1668C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.265C>T
  hgvsp: ENSP00000414537.2:p.Arg89Trp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.127C>T
  hgvsp: ENSP00000345553.6:p.Arg43Trp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.265C>T
  hgvsp: ENSP00000366521.1:p.Arg89Trp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.265C>T
  hgvsp: ENSP00000245957.5:p.Arg89Trp
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg89Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS

20-20051622-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051622
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051622
    reference: chr 20
allele count: 4
allele frequency: 3.304692663582287e-5
allele num: 121040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.268G>C
  hgvsp: ENSP00000366518.2:p.Glu90Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*257G>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.268G>C
  hgvsp: ENSP00000245957.5:p.Glu90Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.268G>C
  hgvsp: ENSP00000366521.1:p.Glu90Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.130G>C
  hgvsp: ENSP00000345553.6:p.Glu44Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.268G>C
  hgvsp: ENSP00000414537.2:p.Glu90Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.268G>C
  hgvsp: ENSP00000417086.1:p.Glu90Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1665G>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1665G>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu90Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-20051623-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051623
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051623
    reference: chr 20
allele count: 6
allele frequency: 4.95703899537343e-5
allele num: 121040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.269A>C
  hgvsp: ENSP00000366521.1:p.Glu90Ala
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.269A>C
  hgvsp: ENSP00000245957.5:p.Glu90Ala
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*258A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.269A>C
  hgvsp: ENSP00000414537.2:p.Glu90Ala
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.269A>C
  hgvsp: ENSP00000366518.2:p.Glu90Ala
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.269A>C
  hgvsp: ENSP00000417086.1:p.Glu90Ala
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1664A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1664A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.131A>C
  hgvsp: ENSP00000345553.6:p.Glu44Ala
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3444
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu90Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

20-20051627-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051627
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051627
    reference: chr 20
allele count: 7
allele frequency: 5.789717461787865e-5
allele num: 120904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.273C>T
  hgvsp: ENST00000475466.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.135C>T
  hgvsp: ENST00000340348.6:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.273C>T
  hgvsp: ENST00000245957.5:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*262C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1660C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.273C>T
  hgvsp: ENST00000451767.2:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.273C>T
  hgvsp: ENST00000377306.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.273C>T
  hgvsp: ENST00000377303.2:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1660C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2386
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2764
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu91Leu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

20-20051628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051628
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051628
    reference: chr 20
allele count: 7
allele frequency: 5.791346074294697e-5
allele num: 120870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.274G>A
  hgvsp: ENSP00000417086.1:p.Asp92Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.274G>A
  hgvsp: ENSP00000414537.2:p.Asp92Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.274G>A
  hgvsp: ENSP00000366518.2:p.Asp92Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.274G>A
  hgvsp: ENSP00000245957.5:p.Asp92Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1659G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.274G>A
  hgvsp: ENSP00000366521.1:p.Asp92Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*263G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1659G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.136G>A
  hgvsp: ENSP00000345553.6:p.Asp46Asn
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp92Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

20-20051635-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051635
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051635
    reference: chr 20
allele count: 64
allele frequency: 5.306447333510214e-4
allele num: 120608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.281A>G
  hgvsp: ENSP00000366521.1:p.Asp94Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.281A>G
  hgvsp: ENSP00000414537.2:p.Asp94Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.281A>G
  hgvsp: ENSP00000245957.5:p.Asp94Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.281A>G
  hgvsp: ENSP00000366518.2:p.Asp94Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.143A>G
  hgvsp: ENSP00000345553.6:p.Asp48Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*270A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1652A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.281A>G
  hgvsp: ENSP00000417086.1:p.Asp94Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1652A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp94Gly
num of homozygotes: 1
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

20-20051636-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051636
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051636
    reference: chr 20
allele count: 3
allele frequency: 2.489378651088688e-5
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.144C>T
  hgvsp: ENST00000340348.6:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.282C>T
  hgvsp: ENST00000451767.2:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.282C>T
  hgvsp: ENST00000377306.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.282C>T
  hgvsp: ENST00000245957.5:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1651C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*271C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1651C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.282C>T
  hgvsp: ENST00000475466.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.282C>T
  hgvsp: ENST00000377303.2:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp94Asp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

20-20051644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051644
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051644
    reference: chr 20
allele count: 1
allele frequency: 8.323622440486099e-6
allele num: 120140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.290G>A
  hgvsp: ENSP00000414537.2:p.Cys97Tyr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1643G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.290G>A
  hgvsp: ENSP00000366518.2:p.Cys97Tyr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*279G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.290G>A
  hgvsp: ENSP00000245957.5:p.Cys97Tyr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.290G>A
  hgvsp: ENSP00000417086.1:p.Cys97Tyr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.152G>A
  hgvsp: ENSP00000345553.6:p.Cys51Tyr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1643G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.290G>A
  hgvsp: ENSP00000366521.1:p.Cys97Tyr
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys97Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/20-20051664-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051664
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051664
    reference: chr 20
allele count: 113
allele frequency: 9.489418878065166e-4
allele num: 119080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*283+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1639+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.294+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.294+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.294+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.156+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.294+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.294+16C>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1639+16C>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 13221
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 31488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2360
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2458
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

20-20051672-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051672
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051672
    reference: chr 20
allele count: 1
allele frequency: 8.419492809753141e-6
allele num: 118772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.294+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.294+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.294+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.294+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*283+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.294+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1639+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.156+24G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1639+24G>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7079
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

20-20051682-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051682
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051682
    reference: chr 20
allele count: 2
allele frequency: 1.692448295704566e-5
allele num: 118172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1639+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.156+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.294+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.294+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.294+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1639+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.294+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*283+34C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.294+34C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6943
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

20-20051687-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051687
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051687
    reference: chr 20
allele count: 1
allele frequency: 8.484354849657232e-6
allele num: 117864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*283+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.294+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.294+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.294+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1639+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1639+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.294+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.294+39A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.156+39A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6859
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4773
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

20-20051693-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051693
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051692
    reference: chr 20
allele count: 155
allele frequency: 1.322345072345072e-3
allele num: 117216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1639+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1639+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.294+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*283+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.294+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.156+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.294+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.294+49delG
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.294+49delG
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28399
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 27072
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2442
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 2
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: AG
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/20-20051693-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051693
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051693
    reference: chr 20
allele count: 1
allele frequency: 8.531258531258532e-6
allele num: 117216
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.294+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1639+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.294+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.294+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.294+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.294+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.156+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1639+45A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*283+45A>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27072
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1064
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

20-20051700-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20051700
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20051700
    reference: chr 20
allele count: 1
allele frequency: 8.580303056303948e-6
allele num: 116546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.156+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*283+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1639+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.294+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.294+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.294+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.294+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1639+52G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.294+52G>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6559
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

20-20054896-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054896
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054896
    reference: chr 20
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-50A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-50A>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10592
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

20-20054900-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054900
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054900
    reference: chr 20
allele count: 47
allele frequency: 3.873349705790246e-4
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-46C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-46C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10592
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2291
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

20-20054905-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054905
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054905
    reference: chr 20
allele count: 1198
allele frequency: 9.870643486858366e-3
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-41A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-41A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 8.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 6.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6678
  bin: 4.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 3.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 5.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 5.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 4.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 9.75e1
  variant carriers: 383
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 6.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 8.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 7.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5790
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4210
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 64
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

20-20054909-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054909
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054909
    reference: chr 20
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-37A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-37A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9093
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

20-20054915-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054915
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054915
    reference: chr 20
allele count: 6
allele frequency: 4.94323518265254e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-31C>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-31C>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8978
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10650
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26671
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

20-20054924-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054924
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054924
    reference: chr 20
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-22C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-22C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9191
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

20-20054929-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054929
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054929
    reference: chr 20
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-17T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-17T>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

20-20054932-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054932
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054932
    reference: chr 20
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-14C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-14C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

20-20054941-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054941
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054941
    reference: chr 20
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.157-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1638-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.295-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.295-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1638-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.295-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.295-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-18-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*284-5T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.295-5T>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 7.25e1
  variant carriers: 0
hgvs: c.295-5T>G
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

20-20054956-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054956
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054956
    reference: chr 20
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.305C>T
  hgvsp: ENSP00000366518.2:p.Thr102Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.167C>T
  hgvsp: ENSP00000345553.6:p.Thr56Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.305C>T
  hgvsp: ENSP00000414537.2:p.Thr102Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.305C>T
  hgvsp: ENSP00000245957.5:p.Thr102Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*294C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.305C>T
  hgvsp: ENSP00000366521.1:p.Thr102Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.305C>T
  hgvsp: ENSP00000417086.1:p.Thr102Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1628C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1628C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9234
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr102Met
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

20-20054957-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054957
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054957
    reference: chr 20
allele count: 6
allele frequency: 4.942176534545814e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1627G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.306G>A
  hgvsp: ENST00000451767.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.306G>A
  hgvsp: ENST00000377306.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.-7G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.306G>A
  hgvsp: ENST00000377303.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.168G>A
  hgvsp: ENST00000340348.6:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*295G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1627G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.306G>A
  hgvsp: ENST00000245957.5:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.306G>A
  hgvsp: ENST00000475466.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4975
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr102Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

20-20054965-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054965
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054965
    reference: chr 20
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.314T>C
  hgvsp: ENSP00000366518.2:p.Met105Thr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.2T>C
  hgvsp: ENSP00000420498.1:p.Met1?
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.314T>C
  hgvsp: ENSP00000366521.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.314T>C
  hgvsp: ENSP00000414537.2:p.Met105Thr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*303T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.314T>C
  hgvsp: ENSP00000417086.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.314T>C
  hgvsp: ENSP00000245957.5:p.Met105Thr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.176T>C
  hgvsp: ENSP00000345553.6:p.Met59Thr
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1619T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1619T>C
  variant of: http://identifiers.org/hgnc/15872
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

20-20054981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054981
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054981
    reference: chr 20
allele count: 11
allele frequency: 9.06065698000066e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1603C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.330C>T
  hgvsp: ENST00000451767.2:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.330C>T
  hgvsp: ENST00000475466.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.330C>T
  hgvsp: ENST00000377306.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.330C>T
  hgvsp: ENST00000245957.5:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.18C>T
  hgvsp: ENST00000472660.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.330C>T
  hgvsp: ENST00000377303.2:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.192C>T
  hgvsp: ENST00000340348.6:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1603C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*319C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala110Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

20-20054982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054982
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054982
    reference: chr 20
allele count: 4
allele frequency: 3.294784356363876e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*320G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.19G>A
  hgvsp: ENSP00000420498.1:p.Val7Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.193G>A
  hgvsp: ENSP00000345553.6:p.Val65Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1602G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.331G>A
  hgvsp: ENSP00000414537.2:p.Val111Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.331G>A
  hgvsp: ENSP00000417086.1:p.Val111Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1602G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.331G>A
  hgvsp: ENSP00000366518.2:p.Val111Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.331G>A
  hgvsp: ENSP00000245957.5:p.Val111Met
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.331G>A
  hgvsp: ENSP00000366521.1:p.Val111Met
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val111Met
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

20-20054985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054985
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054985
    reference: chr 20
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.334G>A
  hgvsp: ENSP00000245957.5:p.Asp112Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.22G>A
  hgvsp: ENSP00000420498.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.196G>A
  hgvsp: ENSP00000345553.6:p.Asp66Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1599G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.334G>A
  hgvsp: ENSP00000366521.1:p.Asp112Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.334G>A
  hgvsp: ENSP00000414537.2:p.Asp112Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.334G>A
  hgvsp: ENSP00000417086.1:p.Asp112Asn
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1599G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*323G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.334G>A
  hgvsp: ENSP00000366518.2:p.Asp112Asn
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp112Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

20-20054986-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054986
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054986
    reference: chr 20
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1598A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.335A>G
  hgvsp: ENSP00000366521.1:p.Asp112Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.197A>G
  hgvsp: ENSP00000345553.6:p.Asp66Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.335A>G
  hgvsp: ENSP00000245957.5:p.Asp112Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1598A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.335A>G
  hgvsp: ENSP00000414537.2:p.Asp112Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.335A>G
  hgvsp: ENSP00000366518.2:p.Asp112Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.335A>G
  hgvsp: ENSP00000417086.1:p.Asp112Gly
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*324A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.23A>G
  hgvsp: ENSP00000420498.1:p.Asp8Gly
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp112Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

20-20054987-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054987
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054987
    reference: chr 20
allele count: 7
allele frequency: 5.765872623636783e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.336T>A
  hgvsp: ENSP00000414537.2:p.Asp112Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.336T>A
  hgvsp: ENSP00000366518.2:p.Asp112Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1597T>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1597T>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.336T>A
  hgvsp: ENSP00000245957.5:p.Asp112Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.198T>A
  hgvsp: ENSP00000345553.6:p.Asp66Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.336T>A
  hgvsp: ENSP00000417086.1:p.Asp112Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*325T>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.24T>A
  hgvsp: ENSP00000420498.1:p.Asp8Glu
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.336T>A
  hgvsp: ENSP00000366521.1:p.Asp112Glu
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp112Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

20-20054990-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20054990
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20054990
    reference: chr 20
allele count: 20
allele frequency: 1.647419317638919e-4
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.27G>C
  hgvsp: ENSP00000420498.1:p.Glu9Asp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.201G>C
  hgvsp: ENSP00000345553.6:p.Glu67Asp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.339G>C
  hgvsp: ENSP00000414537.2:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.339G>C
  hgvsp: ENSP00000417086.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.339G>C
  hgvsp: ENSP00000245957.5:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*328G>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.339G>C
  hgvsp: ENSP00000366521.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.339G>C
  hgvsp: ENSP00000366518.2:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1594G>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1594G>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu113Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

20-20055005-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055005
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055005
    reference: chr 20
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.216T>C
  hgvsp: ENST00000340348.6:c.216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.42T>C
  hgvsp: ENST00000472660.1:c.42T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1579T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*343T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.354T>C
  hgvsp: ENST00000475466.1:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.354T>C
  hgvsp: ENST00000451767.2:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.354T>C
  hgvsp: ENST00000377306.1:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1579T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.354T>C
  hgvsp: ENST00000377303.2:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.354T>C
  hgvsp: ENST00000245957.5:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2770
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys118Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

20-20055015-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055015
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055015
    reference: chr 20
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.364A>G
  hgvsp: ENSP00000417086.1:p.Ile122Val
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.364A>G
  hgvsp: ENSP00000414537.2:p.Ile122Val
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.364A>G
  hgvsp: ENSP00000245957.5:p.Ile122Val
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.226A>G
  hgvsp: ENSP00000345553.6:p.Ile76Val
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1569A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.364A>G
  hgvsp: ENSP00000366518.2:p.Ile122Val
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*353A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.52A>G
  hgvsp: ENSP00000420498.1:p.Ile18Val
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1569A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.364A>G
  hgvsp: ENSP00000366521.1:p.Ile122Val
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2769
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile122Val
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

20-20055020-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055020
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055020
    reference: chr 20
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1564T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1564T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.369T>G
  hgvsp: ENST00000245957.5:c.369T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.369T>G
  hgvsp: ENST00000475466.1:c.369T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*358T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.231T>G
  hgvsp: ENST00000340348.6:c.231T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.369T>G
  hgvsp: ENST00000451767.2:c.369T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.369T>G
  hgvsp: ENST00000377303.2:c.369T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.57T>G
  hgvsp: ENST00000472660.1:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.369T>G
  hgvsp: ENST00000377306.1:c.369T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.369T>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

20-20055021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055021
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055021
    reference: chr 20
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.370C>T
  hgvsp: ENSP00000417086.1:p.Arg124Ter
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.370C>T
  hgvsp: ENSP00000414537.2:p.Arg124Ter
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.232C>T
  hgvsp: ENSP00000345553.6:p.Arg78Ter
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.370C>T
  hgvsp: ENSP00000366518.2:p.Arg124Ter
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.58C>T
  hgvsp: ENSP00000420498.1:p.Arg20Ter
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.370C>T
  hgvsp: ENSP00000366521.1:p.Arg124Ter
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1563C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1563C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*359C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.370C>T
  hgvsp: ENSP00000245957.5:p.Arg124Ter
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg124Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

20-20055022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055022
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055022
    reference: chr 20
allele count: 12
allele frequency: 9.885167306456661e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371G>A
  hgvsp: ENSP00000245957.5:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371G>A
  hgvsp: ENSP00000417086.1:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371G>A
  hgvsp: ENSP00000366521.1:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371G>A
  hgvsp: ENSP00000414537.2:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371G>A
  hgvsp: ENSP00000366518.2:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59G>A
  hgvsp: ENSP00000420498.1:p.Arg20Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420438
  ensembl transcript: ENST00000494029
  gene symbol: C20orf26
  hgvsc: ENST00000494029.1:c.*360G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233G>A
  hgvsp: ENSP00000345553.6:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562G>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg124Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

20-20055025-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055025
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055025
    reference: chr 20
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+3G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+3G>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: c.371+3G>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-20055033-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055033
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055033
    reference: chr 20
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+11A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+11A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5911
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

20-20055034-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055034
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055034
    reference: chr 20
allele count: 317
allele frequency: 2.611417744460005e-3
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+12T>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+12T>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9655
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10620
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 9.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6664
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 7.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4960
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5895
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9204
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 5
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

20-20055035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055035
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055035
    reference: chr 20
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+13G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+13G>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26543
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

20-20055038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055038
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055038
    reference: chr 20
allele count: 15
allele frequency: 1.235849522962084e-4
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+16C>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+16C>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 9239
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4564
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

20-20055039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055039
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055039
    reference: chr 20
allele count: 11
allele frequency: 9.06259783486299e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+17G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+17G>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26535
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

20-20055039-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055039
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055039
    reference: chr 20
allele count: 4
allele frequency: 3.29549012176836e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+17G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+17G>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9237
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

20-20055053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055053
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055053
    reference: chr 20
allele count: 3
allele frequency: 2.47239162683369e-5
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+31A>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+31A>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

20-20055066-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055066
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055066
    reference: chr 20
allele count: 2
allele frequency: 1.648886177387175e-5
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+44T>G
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+44T>G
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5381
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4542
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/20-20055073-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055073
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055073
    reference: chr 20
allele count: 2
allele frequency: 1.650246711883427e-5
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.371+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.233+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.371+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1562+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.371+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.371+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1562+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.371+51A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.59+51A>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26491
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4768
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

20-20055785-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055785
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055785
    reference: chr 20
allele count: 15
allele frequency: 1.236705416769726e-4
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.60-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.372-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1561-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1561-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.372-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.372-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.234-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.372-48G>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.372-48G>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9739
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2072
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3667
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

20-20055800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055800
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055800
    reference: chr 20
allele count: 4081
allele frequency: 3.363609389423711e-2
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.372-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1561-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.372-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.60-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.234-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1561-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.372-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.372-33G>A
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.372-33G>A
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.75e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 8.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 4.25e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9595
  bin: 3.75e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 7.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 5.25e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 3.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 6.25e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.25e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 9.75e1
  variant carriers: 843
genotype depth: GenotypeDepth
  all individuals: 7956
  bin: 4.75e1
  variant carriers: 255
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 260
genotype quality: GenotypeQuality
  all individuals: 3594
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 36095
  bin: 9.75e1
  variant carriers: 3338
genotype quality: GenotypeQuality
  all individuals: 3202
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4585
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4068
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 714
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

20-20055805-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055805
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055805
    reference: chr 20
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366521
  ensembl transcript: ENST00000377306
  gene symbol: C20orf26
  hgvsc: ENST00000377306.1:c.372-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1561-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000417086
  ensembl transcript: ENST00000475466
  gene symbol: C20orf26
  hgvsc: ENST00000475466.1:c.372-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000374307
  ensembl transcript: ENST00000389656
  gene symbol: C20orf26
  hgvsc: ENST00000389656.3:c.-1561-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.60-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000245957
  ensembl transcript: ENST00000245957
  gene symbol: C20orf26
  hgvsc: ENST00000245957.5:c.372-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000414537
  ensembl transcript: ENST00000451767
  gene symbol: C20orf26
  hgvsc: ENST00000451767.2:c.372-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.234-28A>T
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366518
  ensembl transcript: ENST00000377303
  gene symbol: C20orf26
  hgvsc: ENST00000377303.2:c.372-28A>T
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2650
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/20-20055813-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20055813
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 20055813
    reference: chr 20
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000345553
  ensembl transcript: ENST00000340348
  gene symbol: C20orf26
  hgvsc: ENST00000340348.6:c.234-20A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000366524
  ensembl transcript: ENST00000377309
  gene symbol: C20orf26
  hgvsc: ENST00000377309.2:c.-1561-20A>C
  variant of: http://identifiers.org/hgnc/15872
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089101
  ensembl protein: ENSP00000420498
  ensembl transcript: ENST00000472660
  gene symbol: C20orf26
  hgvsc: ENST00000472660.1:c.60-20A>C
  variant of: http://identifiers.org/hgnc/15872
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 643
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2191
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.020408163265306e-2
allele num: 196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.95e-2

FS
type: SiteQuality
SIO_000300: 9.13e-1

QD
type: SiteQuality
SIO_000300: 1.436e1

DP
type: SiteQuality
SIO_000300: 2.02264e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31438
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.784524365561264e-5
allele num: 64230
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.80126738250308e-5
allele num: 11362
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12890
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

FS
type: SiteQuality
SIO_000300: 5.887e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 1.47583e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.87e-1

QD
type: SiteQuality
SIO_000300: 1.01e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.242e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
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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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13114
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64430
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.790436005625879e-5
allele num: 11376
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

DP
type: SiteQuality
SIO_000300: 1.484556e6

QD
type: SiteQuality
SIO_000300: 9.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.33e-1

FS
type: SiteQuality
SIO_000300: 1.431e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 7.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 34407
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
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
all individuals: 274
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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: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2323
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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: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.324500232450023e-4
allele num: 8604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.837e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 1.521495e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.931e1

VQSLOD
type: SiteQuality
SIO_000300: -8.567e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4671
bin: 9.75e1
variant carriers: 1

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
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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: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527650473571647e-5
allele num: 65460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14402
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.287e-1

FS
type: SiteQuality
SIO_000300: 1.955e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.530875e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.559e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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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bin: 4.75e1
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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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65928
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15242
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.027e0

QD
type: SiteQuality
SIO_000300: 1.539e1

DP
type: SiteQuality
SIO_000300: 1.549383e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.354e0

GenotypeQuality
all individuals: 150
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65978
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.509569066527795e-5
allele num: 15362
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.865e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.614e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.12e-1

DP
type: SiteQuality
SIO_000300: 1.552392e6

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

GenotypeQuality
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GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15432
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66014
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.45e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

FS
type: SiteQuality
SIO_000300: 2.656e0

QD
type: SiteQuality
SIO_000300: 1.307e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.801e0

DP
type: SiteQuality
SIO_000300: 1.554175e6

VQSLOD
type: SiteQuality
SIO_000300: 6.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4703
bin: 9.75e1
variant carriers: 23

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1234
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.213802670365875e-3
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.205872599559857e-4
allele num: 66342
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

DP
type: SiteQuality
SIO_000300: 1.567673e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.582e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 1.21e1

GenotypeQuality
all individuals: 382
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.736e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 1.571635e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.892e1

FS
type: SiteQuality
SIO_000300: 2.225e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

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

GenotypeQuality
all individuals: 7331
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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: 3
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 599

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3399
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00724746639401e-5
allele num: 66506
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.126321261479813e-3
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 611
allele frequency: 5.873870409536627e-2
allele num: 10402
num of homozygotes: 27

South Asian
type: Population
allele count: 2
allele frequency: 1.22684333210649e-4
allele num: 16302
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.601393e6

QD
type: SiteQuality
SIO_000300: 1.414e1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.710000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.507e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
all individuals: 4755
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7418
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.018e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.594e1

DP
type: SiteQuality
SIO_000300: 1.584854e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.084e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: 9.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

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

GenotypeQuality
all individuals: 4756
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 7415
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003544182134919e-5
allele num: 66588
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 8.518000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.578e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.798e0

DP
type: SiteQuality
SIO_000300: 1.585328e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4758
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variant carriers: 2

GenotypeQuality
all individuals: 2780
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003003003003003e-5
allele num: 66600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
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: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.62e-1

DP
type: SiteQuality
SIO_000300: 1.585526e6

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.646e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.258e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
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: 10404
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: -1.041e0

DP
type: SiteQuality
SIO_000300: 1.586379e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.788e0

QD
type: SiteQuality
SIO_000300: 8.449999999999999e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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: 16
bin: 3.25e1
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GenotypeQuality
all individuals: 13
bin: 2.75e1
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
all individuals: 2781
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variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.06134076857801e-4
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

QD
type: SiteQuality
SIO_000300: 1.182e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

DP
type: SiteQuality
SIO_000300: 1.58886e6

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4761
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.75e1
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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

DP
type: SiteQuality
SIO_000300: 1.588393e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.276e1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.868e0

MQ
type: SiteQuality
SIO_000300: 5.752e1

GenotypeQuality
all individuals: 2770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 7.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.222195062331948e-4
allele num: 16364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 2
allele frequency: 3.002011347602894e-5
allele num: 66622
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.587005e6

QD
type: SiteQuality
SIO_000300: 1.078e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 2.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.833292593497922e-4
allele num: 16364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 908
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.078e1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

DP
type: SiteQuality
SIO_000300: 1.587005e6

FS
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 7
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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: 2771
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3443
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.457216940363008e-4
allele num: 11570
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.684e0

FS
type: SiteQuality
SIO_000300: 1.3457e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

DP
type: SiteQuality
SIO_000300: 1.584953e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

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

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4766
bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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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: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1251
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.767012687427913e-4
allele num: 10404
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 16302
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.762e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 3.342e0

DP
type: SiteQuality
SIO_000300: 1.58519e6

QD
type: SiteQuality
SIO_000300: 1.054e1

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
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GenotypeQuality
all individuals: 96
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1251
bin: 9.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4767
bin: 9.75e1
variant carriers: 7

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.728181468665898e-4
allele num: 10404
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: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 1.583222e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

GenotypeQuality
all individuals: 465
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36767
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
bin: 2.75e1
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GenotypeQuality
all individuals: 2761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.009615384615385e-5
allele num: 66560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16176
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.588e0

QD
type: SiteQuality
SIO_000300: 1.266e1

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.8e-1

FS
type: SiteQuality
SIO_000300: 4.214e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

DP
type: SiteQuality
SIO_000300: 1.582626e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 2752
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GenotypeQuality
all individuals: 764
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 1249
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 2379
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GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 39
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GenotypeQuality
all individuals: 88
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GenotypeQuality
all individuals: 7321
bin: 6.75e1
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GenotypeQuality
all individuals: 4812
bin: 9.75e1
variant carriers: 63

GenotypeQuality
all individuals: 1003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36364
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 64
allele frequency: 6.152662949432801e-3
allele num: 10402
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15992
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.32e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.5798e6

QD
type: SiteQuality
SIO_000300: 1.337e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.81e-1

GenotypeQuality
all individuals: 1252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7314
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36086
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4772
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008966720828068e-5
allele num: 66468
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.282196255811031e-5
allele num: 15918
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.575591e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.715e0

QD
type: SiteQuality
SIO_000300: 1.201e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.142e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
all individuals: 35543
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
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
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3427
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.384065372829418e-5
allele num: 15664
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.26e-1

DP
type: SiteQuality
SIO_000300: 1.566635e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.039e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.988e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.69e-1

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
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: 4846
bin: 9.75e1
variant carriers: 113

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: 1002
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 6
allele frequency: 5.197505197505198e-4
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51372952680815e-5
allele num: 66062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

African
type: Population
allele count: 106
allele frequency: 1.020801232665639e-2
allele num: 10384
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.543308e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.204e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

GenotypeQuality
all individuals: 4775
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 810
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 108
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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: 128
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2702
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variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
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variant carriers: 0

GenotypeQuality
all individuals: 2370
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515840533575868e-5
allele num: 65970
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.530556e6

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: 2.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

QD
type: SiteQuality
SIO_000300: 9.77e0

FS
type: SiteQuality
SIO_000300: 1.972e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.955e0

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

GenotypeQuality
all individuals: 295
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4775
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 234
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variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30892
bin: 6.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038497766704142e-5
allele num: 65822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14358
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.518304e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.386e0

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

FS
type: SiteQuality
SIO_000300: 3.084e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 1.518e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
all individuals: 285
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1040
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52008026023774e-5
allele num: 65786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14094
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.510862e6

QD
type: SiteQuality
SIO_000300: 1.293e1

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 1.379e0

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 924
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2645
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1246
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 295
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4916
bin: 9.75e1
variant carriers: 150

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6724
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.164634146341463e-4
allele num: 65600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13682
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.424657534246575e-3
allele num: 876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 103
allele frequency: 1.559188616409325e-2
allele num: 6606
num of homozygotes: 2

DP
type: SiteQuality
SIO_000300: 1.505235e6

VQSLOD
type: SiteQuality
SIO_000300: 6.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.01e-2

QD
type: SiteQuality
SIO_000300: 1.34e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1565
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 363
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GenotypeQuality
all individuals: 1590
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.30887297178775e-5
allele num: 13682
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65600
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.01e-2

DP
type: SiteQuality
SIO_000300: 1.505235e6

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

QD
type: SiteQuality
SIO_000300: 1.34e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

GenotypeQuality
all individuals: 915
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
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GenotypeQuality
all individuals: 22179
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variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4819
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1262
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528818223513224e-5
allele num: 65410
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.514699e6

MQRankSum
type: SiteQuality
SIO_000300: -3.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

FS
type: SiteQuality
SIO_000300: 3.005e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.228e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.095e0

QD
type: SiteQuality
SIO_000300: 1.82e0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
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GenotypeQuality
all individuals: 109
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 78
bin: 3.75e1
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GenotypeQuality
all individuals: 2
bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27056
bin: 9.75e1
variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.368e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.27e1

DP
type: SiteQuality
SIO_000300: 3.112226e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.75e1
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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bin: 2.5e0
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GenotypeQuality
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variant carriers: 47

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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2712
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497211728728189e-5
allele num: 66708
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.57537566650509e-3
allele num: 16504
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 17
allele frequency: 1.470588235294118e-3
allele num: 11560
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.163e0

DP
type: SiteQuality
SIO_000300: 3.113653e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.51e1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

GenotypeQuality
all individuals: 27131
bin: 9.75e1
variant carriers: 1132

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4486
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variant carriers: 1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 8894
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 2282
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4908
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variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 1142
allele frequency: 1.097443782433212e-1
allele num: 10406
num of homozygotes: 64

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 36
allele frequency: 3.113109650639917e-3
allele num: 11564
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: 14
allele frequency: 2.098321342925659e-4
allele num: 66720
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.405286343612335e-3
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.32e0

DP
type: SiteQuality
SIO_000300: 3.131001e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.950000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

QD
type: SiteQuality
SIO_000300: 1.718e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

GenotypeQuality
all individuals: 26668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 2320
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variant carriers: 0

GenotypeQuality
all individuals: 5867
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 2768
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variant carriers: 0

GenotypeQuality
all individuals: 4554
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
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: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.497e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.823e1

DP
type: SiteQuality
SIO_000300: 3.099273e6

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9130
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 4552
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
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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
all individuals: 26
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 4266
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

DP
type: SiteQuality
SIO_000300: 3.099977e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.424e1

FS
type: SiteQuality
SIO_000300: 3.533e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4971
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 3.10063e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 6.84e0

QD
type: SiteQuality
SIO_000300: 1.294e1

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 26671
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variant carriers: 1

GenotypeQuality
all individuals: 5888
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.100795e6

FS
type: SiteQuality
SIO_000300: 9.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 6.71e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.342e1

GenotypeQuality
all individuals: 4267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 5890
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 4555
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GenotypeQuality
all individuals: 0
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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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African
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European (Non-Finnish)
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Other
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South Asian
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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MQRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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Other
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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MQ
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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Latino
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QD
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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East Asian
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African
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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African
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Other
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FS
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MQRankSum
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QD
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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DP
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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Latino
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South Asian
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East Asian
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European (Finnish)
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.15e0

QD
type: SiteQuality
SIO_000300: 1.126e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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: 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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2769
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.292e1

FS
type: SiteQuality
SIO_000300: 4.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

DP
type: SiteQuality
SIO_000300: 3.101032e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.59e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.75e1
variant carriers: 7

East Asian
type: Population
allele count: 7
allele frequency: 8.092485549132948e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

DP
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SIO_000300: 3.101325e6

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.265e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 26648
bin: 9.75e1
variant carriers: 20

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

African
type: Population
allele count: 20
allele frequency: 1.921968095329617e-3
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.23e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e0

DP
type: SiteQuality
SIO_000300: 3.102147e6

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.047e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.59e-1

VQSLOD
type: SiteQuality
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DP
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SIO_000300: 3.100621e6

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.8e0

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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QD
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MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.682e-1

FS
type: SiteQuality
SIO_000300: 5.206e0

ClippingRankSum
type: SiteQuality
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GenotypeDepth
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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: 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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.21e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4973
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.498621268433042e-4
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.36e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

DP
type: SiteQuality
SIO_000300: 3.101029e6

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.325e1

DP
type: SiteQuality
SIO_000300: 3.100369e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.593e0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.515e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

FS
type: SiteQuality
SIO_000300: 2.464e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

DP
type: SiteQuality
SIO_000300: 3.100287e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e0

QD
type: SiteQuality
SIO_000300: 1.401e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 312

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 313
allele frequency: 1.895591085271318e-2
allele num: 16512
num of homozygotes: 5

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.197e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

FS
type: SiteQuality
SIO_000300: 7.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

QD
type: SiteQuality
SIO_000300: 1.277e1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

DP
type: SiteQuality
SIO_000300: 3.111737e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 2319
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -8.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.198e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.254e0

VQSLOD
type: SiteQuality
SIO_000300: -4.094e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

DP
type: SiteQuality
SIO_000300: 3.099253e6

QD
type: SiteQuality
SIO_000300: 1.355e1

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 26544
bin: 9.75e1
variant carriers: 15

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 13
allele frequency: 1.94838284224094e-4
allele num: 66722
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 3.099685e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

FS
type: SiteQuality
SIO_000300: 3.024e0

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.246417013407304e-4
allele num: 8652
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.963e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.666e0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

DP
type: SiteQuality
SIO_000300: 3.09935e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
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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: 66720
num of homozygotes: 0

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

African
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allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
all individuals: 2309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4911
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 262
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26495
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 2.149e0

DP
type: SiteQuality
SIO_000300: 3.073839e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e0

QD
type: SiteQuality
SIO_000300: 1.588e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.008e-1

GenotypeQuality
all individuals: 2305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4503
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4525
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

East Asian
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: 6596
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.049709e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 6.632e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.113e0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35545
bin: 9.75e1
variant carriers: 15

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

GenotypeQuality
all individuals: 4245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2619
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

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

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.093113482056256e-4
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.855824e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.3e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.27e0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2562
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4305
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2037
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 177
allele frequency: 1.530877010897769e-2
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 3737
allele frequency: 3.59119738612339e-1
allele num: 10406
num of homozygotes: 713

South Asian
type: Population
allele count: 12
allele frequency: 7.270964614638875e-4
allele num: 16504
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 1.324503311258278e-2
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 143
allele frequency: 2.143928035982009e-3
allele num: 66700
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 6.96e-1

QD
type: SiteQuality
SIO_000300: 1.807e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.228e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.951e-1

DP
type: SiteQuality
SIO_000300: 2.917866e6

VQSLOD
type: SiteQuality
SIO_000300: 1.29e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3412
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4517
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34827
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4932
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.053e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.134e1

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 5.479e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

DP
type: SiteQuality
SIO_000300: 2.812322e6