21-33867528-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33867528
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33867528
    reference: chr 21
allele count: 1378
allele frequency: 1.178442540236373e-2
allele num: 116934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-6197G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-6197G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*368+48G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.778+48G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.646+48G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.54+48G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.457+48G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.254+48G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.778+48G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1745+48G>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 2.25e1
  variant carriers: 297
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 2.75e1
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 1.75e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.25e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 3.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 1.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 4.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3912
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.5e0
  variant carriers: 1
num of homozygotes: 37
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

21-33867528-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33867528
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33867528
    reference: chr 21
allele count: 2
allele frequency: 1.710366531547711e-5
allele num: 116934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1745+48G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.778+48G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-6197G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.254+48G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.457+48G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.778+48G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.646+48G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-6197G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*368+48G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.54+48G>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10423
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

21-33873676-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873676
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873676
    reference: chr 21
allele count: 1
allele frequency: 8.985694773919919e-6
allele num: 111288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2560A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-49A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-49A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8998
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5369
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

21-33873693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873693
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873693
    reference: chr 21
allele count: 11
allele frequency: 9.77204484480216e-5
allele num: 112566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2543C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-32C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-32C>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13669
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 9.75e1
  variant carriers: 10
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

21-33873694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873694
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873694
    reference: chr 21
allele count: 8
allele frequency: 7.088930634813739e-5
allele num: 112852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2542G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-31G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-31G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2628
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

21-33873701-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873701
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873701
    reference: chr 21
allele count: 1
allele frequency: 8.715204545850691e-6
allele num: 114742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2535A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-24A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-24A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14508
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
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: A
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

21-33873703-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873703
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873703
    reference: chr 21
allele count: 1
allele frequency: 8.677241331435909e-6
allele num: 115244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2533A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-22A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-22A>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46636
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-33873709-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873709
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873709
    reference: chr 21
allele count: 1
allele frequency: 8.612819320276298e-6
allele num: 116106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2527C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-16C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-16C>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

21-33873710-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873710
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873710
    reference: chr 21
allele count: 1
allele frequency: 8.600670852326481e-6
allele num: 116270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-15T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2526T>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

21-33873717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873717
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873717
    reference: chr 21
allele count: 4
allele frequency: 3.420323562609023e-5
allele num: 116948
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2519G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-8G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-8G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15158
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 9.75e1
  variant carriers: 4
hgvs: c.779-8G>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/21-33873718-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873718
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873718
    reference: chr 21
allele count: 1
allele frequency: 8.549054474575111e-6
allele num: 116972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.458-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*369-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*225-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.779-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.635-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2518C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.779-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.647-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1746-7C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.255-7C>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
hgvs: c.779-7C>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

21-33873729-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873729
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873729
    reference: chr 21
allele count: 1
allele frequency: 8.528202766548977e-6
allele num: 117258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1750C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*373C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.783C>G
  hgvsp: ENST00000300255.2:c.783C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.639C>G
  hgvsp: ENST00000401402.3:c.639C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.651C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.462C>G
  hgvsp: ENST00000457807.1:c.462C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2507C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.259C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.783C>G
  hgvsp: ENST00000382699.3:c.783C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*229C>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36677
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro261Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

21-33873733-A-AACAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873733
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873737
    reference: chr 21
allele count: 1
allele frequency: 8.522824123001398e-6
allele num: 117332
alternate allele: AACAT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.646_649dupATAC
  hgvsp: ENSP00000384594.3:p.Leu217HisfsTer6
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.790_793dupATAC
  hgvsp: ENSP00000372146.3:p.Leu265HisfsTer6
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.469_472dupATAC
  hgvsp: ENSP00000401547.1:p.Leu158HisfsTer6
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*236_*239dupATAC
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.658_661dupATAC
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*380_*383dupATAC
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.790_793dupATAC
  hgvsp: ENSP00000300255.2:p.Leu265HisfsTer6
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1757_1760dupATAC
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.266_269dupATAC
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2500_55-2497dupATAC
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu265HisfsTer6
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

21-33873736-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873736
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873736
    reference: chr 21
allele count: 1
allele frequency: 8.521081154776918e-6
allele num: 117356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*380A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1757A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.658A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.790A>G
  hgvsp: ENSP00000372146.3:p.Ile264Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.469A>G
  hgvsp: ENSP00000401547.1:p.Ile157Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.646A>G
  hgvsp: ENSP00000384594.3:p.Ile216Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2500A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*236A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.790A>G
  hgvsp: ENSP00000300255.2:p.Ile264Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.266A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile264Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/21-33873743-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873743
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873743
    reference: chr 21
allele count: 15
allele frequency: 1.277704901276001e-4
allele num: 117398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.476C>A
  hgvsp: ENSP00000401547.1:p.Thr159Lys
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*243C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.653C>A
  hgvsp: ENSP00000384594.3:p.Thr218Lys
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.273C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.665C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1764C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.797C>A
  hgvsp: ENSP00000300255.2:p.Thr266Lys
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*387C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.797C>A
  hgvsp: ENSP00000372146.3:p.Thr266Lys
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2493C>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15459
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr266Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

21-33873743-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873743
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873743
    reference: chr 21
allele count: 1
allele frequency: 8.518032675173342e-6
allele num: 117398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*387C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.797C>T
  hgvsp: ENSP00000300255.2:p.Thr266Ile
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.476C>T
  hgvsp: ENSP00000401547.1:p.Thr159Ile
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1764C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.273C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.665C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.797C>T
  hgvsp: ENSP00000372146.3:p.Thr266Ile
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2493C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.653C>T
  hgvsp: ENSP00000384594.3:p.Thr218Ile
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36637
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr266Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/21-33873744-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873744
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873744
    reference: chr 21
allele count: 1
allele frequency: 8.517742457539054e-6
allele num: 117402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*244A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.477A>C
  hgvsp: ENST00000457807.1:c.477A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.654A>C
  hgvsp: ENST00000401402.3:c.654A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.798A>C
  hgvsp: ENST00000300255.2:c.798A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1765A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.274A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*388A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2492A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.798A>C
  hgvsp: ENST00000382699.3:c.798A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.666A>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr266Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

21-33873744-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873744
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873744
    reference: chr 21
allele count: 1
allele frequency: 8.517742457539054e-6
allele num: 117402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*388A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.798A>G
  hgvsp: ENST00000382699.3:c.798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.477A>G
  hgvsp: ENST00000457807.1:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*244A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.666A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.654A>G
  hgvsp: ENST00000401402.3:c.654A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.798A>G
  hgvsp: ENST00000300255.2:c.798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2492A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1765A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.274A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr266Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

21-33873746-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873746
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873746
    reference: chr 21
allele count: 5
allele frequency: 4.25930658488798e-5
allele num: 117390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2490C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.800C>T
  hgvsp: ENSP00000300255.2:p.Ala267Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.668C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.276C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*246C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1767C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.479C>T
  hgvsp: ENSP00000401547.1:p.Ala160Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*390C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.656C>T
  hgvsp: ENSP00000384594.3:p.Ala219Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.800C>T
  hgvsp: ENSP00000372146.3:p.Ala267Val
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15484
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala267Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

21-33873748-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873748
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873748
    reference: chr 21
allele count: 1
allele frequency: 8.515131388477325e-6
allele num: 117438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.278A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.658A>T
  hgvsp: ENSP00000384594.3:p.Ile220Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.802A>T
  hgvsp: ENSP00000372146.3:p.Ile268Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.670A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*392A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.481A>T
  hgvsp: ENSP00000401547.1:p.Ile161Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*248A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.802A>T
  hgvsp: ENSP00000300255.2:p.Ile268Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2488A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1769A>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile268Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

21-33873749-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873749
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873749
    reference: chr 21
allele count: 13
allele frequency: 1.106985932763378e-4
allele num: 117436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.671T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2487T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.482T>C
  hgvsp: ENSP00000401547.1:p.Ile161Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*249T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.803T>C
  hgvsp: ENSP00000372146.3:p.Ile268Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.803T>C
  hgvsp: ENSP00000300255.2:p.Ile268Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.279T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.659T>C
  hgvsp: ENSP00000384594.3:p.Ile220Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1770T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*393T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36591
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 9.75e1
  variant carriers: 13
hgvs: p.Ile268Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

21-33873760-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873760
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873760
    reference: chr 21
allele count: 3
allele frequency: 2.556629339878304e-5
allele num: 117342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*404A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.682A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.290A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.814A>T
  hgvsp: ENSP00000300255.2:p.Ile272Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1781A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.670A>T
  hgvsp: ENSP00000384594.3:p.Ile224Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.814A>T
  hgvsp: ENSP00000372146.3:p.Ile272Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.493A>T
  hgvsp: ENSP00000401547.1:p.Ile165Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2476A>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*260A>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile272Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

21-33873761-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873761
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873761
    reference: chr 21
allele count: 5
allele frequency: 4.261629988237901e-5
allele num: 117326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.494T>C
  hgvsp: ENSP00000401547.1:p.Ile165Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.815T>C
  hgvsp: ENSP00000372146.3:p.Ile272Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*405T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.291T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2475T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*261T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.671T>C
  hgvsp: ENSP00000384594.3:p.Ile224Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.815T>C
  hgvsp: ENSP00000300255.2:p.Ile272Thr
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000459833
  gene symbol: EVA1C
  hgvsc: ENST00000459833.1:n.683T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1782T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4790
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile272Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

21-33873781-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873781
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873781
    reference: chr 21
allele count: 1
allele frequency: 8.569127148708632e-6
allele num: 116698
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2455T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.835T>C
  hgvsp: ENST00000300255.2:c.835T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.691T>C
  hgvsp: ENST00000401402.3:c.691T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1802T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*425T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.311T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.835T>C
  hgvsp: ENST00000382699.3:c.835T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.514T>C
  hgvsp: ENST00000457807.1:c.514T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*281T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu279Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

21-33873784-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873784
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873784
    reference: chr 21
allele count: 1
allele frequency: 8.585459665510492e-6
allele num: 116476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1805A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.838A>G
  hgvsp: ENSP00000372146.3:p.Lys280Glu
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*428A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.694A>G
  hgvsp: ENSP00000384594.3:p.Lys232Glu
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.517A>G
  hgvsp: ENSP00000401547.1:p.Lys173Glu
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*284A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.314A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.838A>G
  hgvsp: ENSP00000300255.2:p.Lys280Glu
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2452A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys280Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

21-33873794-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873794
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873794
    reference: chr 21
allele count: 1
allele frequency: 8.721285168582443e-6
allele num: 114662
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.848A>G
  hgvsp: ENSP00000300255.2:p.Asp283Gly
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*294A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1815A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.704A>G
  hgvsp: ENSP00000384594.3:p.Asp235Gly
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.527A>G
  hgvsp: ENSP00000401547.1:p.Asp176Gly
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.848A>G
  hgvsp: ENSP00000372146.3:p.Asp283Gly
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2442A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*438A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.324A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp283Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

21-33873795-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873795
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873795
    reference: chr 21
allele count: 3
allele frequency: 2.616248648271532e-5
allele num: 114668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2441T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.528T>C
  hgvsp: ENST00000457807.1:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.705T>C
  hgvsp: ENST00000401402.3:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*439T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.849T>C
  hgvsp: ENST00000382699.3:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*295T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1816T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.849T>C
  hgvsp: ENST00000300255.2:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.325T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
hgvs: c.849T>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

21-33873804-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873804
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873804
    reference: chr 21
allele count: 2
allele frequency: 1.777840989901863e-5
allele num: 112496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+8T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*448T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1825T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.537T>C
  hgvsp: ENST00000457807.1:c.537T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2432T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.858T>C
  hgvsp: ENST00000300255.2:c.858T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.334T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*304T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.714T>C
  hgvsp: ENST00000401402.3:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15005
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
hgvs: c.858T>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

21-33873810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873810
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873810
    reference: chr 21
allele count: 1
allele frequency: 9.16338312104829e-6
allele num: 109130
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+5T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+5T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+5T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+5T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+5T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+14T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+5T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2426T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.543T>C
  hgvsp: ENST00000457807.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33685
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 3.25e1
  variant carriers: 0
hgvs: c.859+5T>C
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

21-33873814-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873814
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873815
    reference: chr 21
allele count: 1
allele frequency: 9.25823056697404e-6
allele num: 108012
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+10dupA
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+10dupA
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+10dupA
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+10dupA
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2421dupA
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.548dupA
  hgvsp: ENSP00000401547.1:p.Tyr183Ter
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+10dupA
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+10dupA
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+19dupA
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14503
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr183Ter
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

21-33873816-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873816
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873816
    reference: chr 21
allele count: 1
allele frequency: 9.260974254491573e-6
allele num: 107980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+11T>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2420T>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+11T>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+11T>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.549T>A
  hgvsp: ENSP00000401547.1:p.Tyr183Ter
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+20T>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+11T>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+11T>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+11T>A
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr183Ter
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

21-33873816-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873816
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873816
    reference: chr 21
allele count: 1
allele frequency: 9.260974254491573e-6
allele num: 107980
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+11T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.549T>C
  hgvsp: ENST00000457807.1:c.549T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+11T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+11T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2420T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+20T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+11T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+11T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+11T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3729
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr183Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

21-33873821-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873821
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873821
    reference: chr 21
allele count: 1
allele frequency: 9.414777434661444e-6
allele num: 106216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+16T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+16T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+16T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+16T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+16T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.554T>C
  hgvsp: ENSP00000401547.1:p.Leu185Ser
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+25T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2415T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+16T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2775
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2458
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu185Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

21-33873823-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873823
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873823
    reference: chr 21
allele count: 7
allele frequency: 6.637210096144729e-5
allele num: 105466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.556C>T
  hgvsp: ENST00000457807.1:c.556C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+18C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+27C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+18C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+18C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2413C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+18C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+18C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+18C>T
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20398
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3037
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu186Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

21-33873831-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873831
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873831
    reference: chr 21
allele count: 3
allele frequency: 2.923406743324888e-5
allele num: 102620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.564A>G
  hgvsp: ENST00000457807.1:c.564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+26A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+26A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+26A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+26A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2405A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+26A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+26A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+35A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11484
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16335
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala188Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

21-33873833-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873833
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873833
    reference: chr 21
allele count: 1
allele frequency: 9.770777558478104e-6
allele num: 102346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+37T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+28T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+28T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+28T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.566T>G
  hgvsp: ENSP00000401547.1:p.Phe189Cys
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+28T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2403T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+28T>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+28T>G
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11238
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23035
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe189Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

21-33873835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873835
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873835
    reference: chr 21
allele count: 2
allele frequency: 1.967690521634757e-5
allele num: 101642
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+30C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2401C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+30C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+30C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.568C>T
  hgvsp: ENSP00000401547.1:p.Leu190Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+30C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+30C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+30C>T
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15144
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu190Phe
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

21-33873844-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873844
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873844
    reference: chr 21
allele count: 2
allele frequency: 2.013733663585654e-5
allele num: 99318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2392T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+39T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.577T>C
  hgvsp: ENSP00000401547.1:p.Ter193GlnextTer20
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+39T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+39T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+39T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+39T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+39T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+48T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16322
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ter193GlnextTer20
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP

21-33873849-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873849
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873849
    reference: chr 21
allele count: 1
allele frequency: 1.020491468691322e-5
allele num: 97992
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+44G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+44G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+53G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+44G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+44G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2387G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+44G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+44G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+1G>C
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15939
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
hgvs: c.*2+1G>C
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/21-33873855-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873855
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873855
    reference: chr 21
allele count: 1
allele frequency: 1.031310589497133e-5
allele num: 96964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+50A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+50A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+50A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2381A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+59A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+50A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+7A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+50A>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+50A>C
  variant of: http://identifiers.org/hgnc/13239
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9923
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16381
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 5.25e1
  variant carriers: 0
hgvs: c.*2+7A>C
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/21-33873859-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873859
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873859
    reference: chr 21
allele count: 1
allele frequency: 1.042883363924579e-5
allele num: 95888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+63C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+54C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+54C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+11C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2377C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+54C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+54C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+54C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+54C>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20083
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7493
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum

21-33873862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873862
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873862
    reference: chr 21
allele count: 1
allele frequency: 1.046988860038529e-5
allele num: 95512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2374G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+66G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+57G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+57G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+57G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+57G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+14G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+57G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+57G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7556
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4660
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

21-33873873-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873873
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873873
    reference: chr 21
allele count: 1
allele frequency: 1.058245851676261e-5
allele num: 94496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+68G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+68G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+68G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+68G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+77G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+68G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2363G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+68G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+25G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10131
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

21-33873873-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873873
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873873
    reference: chr 21
allele count: 921
allele frequency: 9.746444293938368e-3
allele num: 94496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+77G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2363G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+68G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+68G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+68G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+68G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+68G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+25G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+68G>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 2.25e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 7.5e0
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 10131
  bin: 1.75e1
  variant carriers: 367
genotype depth: GenotypeDepth
  all individuals: 20877
  bin: 1.25e1
  variant carriers: 270
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 2.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.25e1
  variant carriers: 6
num of homozygotes: 23
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

21-33873882-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873882
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873882
    reference: chr 21
allele count: 1
allele frequency: 1.075893529576313e-5
allele num: 92946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2354A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+77A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+77A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+77A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+77A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+86A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+77A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+77A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+34A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13101
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16033
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/21-33873883-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873883
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873883
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 92612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+78C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+78C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+78C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+78C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2353C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+78C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+78C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+87C>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+35C>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20686
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15927
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.5e0
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

21-33873883-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873883
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873883
    reference: chr 21
allele count: 1
allele frequency: 1.07977367943679e-5
allele num: 92612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+78C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+87C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+78C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+78C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2353C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+78C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+78C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+35C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+78C>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15927
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6012
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

21-33873888-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33873888
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33873888
    reference: chr 21
allele count: 1
allele frequency: 1.094906494985328e-5
allele num: 91332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.715+83G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*449+83G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*305+83G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*2+40G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-2348G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.335+83G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.859+83G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1826+83G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.850+92G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8756
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

21-33876185-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876185
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876185
    reference: chr 21
allele count: 1
allele frequency: 8.421478137842754e-6
allele num: 118744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-51G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-51G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2887
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

21-33876186-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876186
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876186
    reference: chr 21
allele count: 107
allele frequency: 9.025879812396666e-4
allele num: 118548
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-50C>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-50C>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3233
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 2
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

21-33876187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876187
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876187
    reference: chr 21
allele count: 3
allele frequency: 2.52691160863193e-5
allele num: 118722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-49G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-49G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

21-33876188-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876188
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876188
    reference: chr 21
allele count: 1
allele frequency: 8.41864224137931e-6
allele num: 118784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-48T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-48T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36910
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

21-33876197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876197
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876197
    reference: chr 21
allele count: 2
allele frequency: 1.683416662458125e-5
allele num: 118806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-39C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-39C>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

21-33876198-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876198
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876198
    reference: chr 21
allele count: 1
allele frequency: 8.407741848694278e-6
allele num: 118938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-38A>G
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-38A>G
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5337
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

21-33876199-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876199
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876199
    reference: chr 21
allele count: 1
allele frequency: 8.407317729351627e-6
allele num: 118944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-37G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-37G>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

21-33876202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876202
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876202
    reference: chr 21
allele count: 1
allele frequency: 8.401243384020834e-6
allele num: 119030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-34G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-34G>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

21-33876203-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876203
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876203
    reference: chr 21
allele count: 6
allele frequency: 5.039560550320012e-5
allele num: 119058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-33T>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-33T>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
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: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

21-33876218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876218
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876218
    reference: chr 21
allele count: 1
allele frequency: 8.365820603342981e-6
allele num: 119534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-18G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-18G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

21-33876218-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876218
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876218
    reference: chr 21
allele count: 1
allele frequency: 8.365820603342981e-6
allele num: 119534
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-18G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-18G>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

21-33876229-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876229
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876229
    reference: chr 21
allele count: 1
allele frequency: 8.319882856049386e-6
allele num: 120194
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827-7G>C
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851-7G>C
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
hgvs: c.860-7G>C
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

21-33876236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876236
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876236
    reference: chr 21
allele count: 1
allele frequency: 8.295588406085643e-6
allele num: 120546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860G>A
  hgvsp: ENSP00000300255.2:p.Gly287Asp
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851G>A
  hgvsp: ENSP00000372146.3:p.Gly284Asp
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716G>A
  hgvsp: ENSP00000384594.3:p.Gly239Asp
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly287Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

21-33876236-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876236
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876236
    reference: chr 21
allele count: 1
allele frequency: 8.295588406085643e-6
allele num: 120546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.55G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1827G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.851G>T
  hgvsp: ENSP00000372146.3:p.Gly284Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*450G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.336G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.716G>T
  hgvsp: ENSP00000384594.3:p.Gly239Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.860G>T
  hgvsp: ENSP00000300255.2:p.Gly287Val
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*306G>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*3G>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly287Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

21-33876246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876246
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876246
    reference: chr 21
allele count: 848
allele frequency: 7.010929774955768e-3
allele num: 120954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.346C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.861C>T
  hgvsp: ENST00000382699.3:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.65C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*316C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*460C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.726C>T
  hgvsp: ENST00000401402.3:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1837C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.870C>T
  hgvsp: ENST00000300255.2:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 9.75e1
  variant carriers: 663
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7002
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 7.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe290Phe
num of homozygotes: 7
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

21-33876247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876247
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876247
    reference: chr 21
allele count: 3
allele frequency: 2.479338842975207e-5
allele num: 121000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*317G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*461G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.871G>A
  hgvsp: ENSP00000300255.2:p.Asp291Asn
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.727G>A
  hgvsp: ENSP00000384594.3:p.Asp243Asn
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.862G>A
  hgvsp: ENSP00000372146.3:p.Asp288Asn
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.66G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.347G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1838G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*14G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp291Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

21-33876254-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876254
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876254
    reference: chr 21
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*468G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1845G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.734G>A
  hgvsp: ENSP00000384594.3:p.Ser245Asn
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*324G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.878G>A
  hgvsp: ENSP00000300255.2:p.Ser293Asn
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.354G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.869G>A
  hgvsp: ENSP00000372146.3:p.Ser290Asn
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.73G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9208
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2938
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser293Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

21-33876255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876255
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876255
    reference: chr 21
allele count: 1248
allele frequency: 1.030246995112931e-2
allele num: 121136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*469C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.870C>T
  hgvsp: ENST00000382699.3:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.879C>T
  hgvsp: ENST00000300255.2:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*325C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.355C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.74C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.735C>T
  hgvsp: ENST00000401402.3:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1846C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*22C>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6225
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 9.75e1
  variant carriers: 1118
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36749
  bin: 9.75e1
  variant carriers: 1215
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser293Ser
num of homozygotes: 32
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

21-33876256-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876256
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876256
    reference: chr 21
allele count: 12
allele frequency: 9.902460761499233e-5
allele num: 121182
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.880G>A
  hgvsp: ENSP00000300255.2:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*326G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.356G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*470G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.871G>A
  hgvsp: ENSP00000372146.3:p.Gly291Arg
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.736G>A
  hgvsp: ENSP00000384594.3:p.Gly246Arg
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*23G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.75G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1847G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly294Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

21-33876260-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876260
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876260
    reference: chr 21
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.740C>T
  hgvsp: ENSP00000384594.3:p.Ser247Leu
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*330C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1851C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.875C>T
  hgvsp: ENSP00000372146.3:p.Ser292Leu
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.360C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*474C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.884C>T
  hgvsp: ENSP00000300255.2:p.Ser295Leu
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.79C>T
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9325
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser295Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

21-33876265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876265
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876265
    reference: chr 21
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000496615
  gene symbol: EVA1C
  hgvsc: ENST00000496615.1:n.365G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000389291
  ensembl transcript: ENST00000437338
  gene symbol: EVA1C
  hgvsc: ENST00000437338.1:c.*479G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000464037
  gene symbol: EVA1C
  hgvsc: ENST00000464037.1:n.1856G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.889G>A
  hgvsp: ENSP00000300255.2:p.Val297Ile
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.745G>A
  hgvsp: ENSP00000384594.3:p.Val249Ile
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000407190
  ensembl transcript: ENST00000435323
  gene symbol: EVA1C
  hgvsc: ENST00000435323.1:c.*335G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166979
  ensembl transcript: ENST00000485488
  gene symbol: EVA1C
  hgvsc: ENST00000485488.1:n.84G>A
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.880G>A
  hgvsp: ENSP00000372146.3:p.Val294Ile
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000401547
  ensembl transcript: ENST00000457807
  gene symbol: EVA1C
  hgvsc: ENST00000457807.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2823
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val297Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

21-33876265-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33876265
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 33876265
    reference: chr 21
allele count: 6
allele frequency: 4.948290365678658e-5
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000384594
  ensembl transcript: ENST00000401402
  gene symbol: EVA1C
  hgvsc: ENST00000401402.3:c.745G>T
  hgvsp: ENSP00000384594.3:p.Val249Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000300255
  ensembl transcript: ENST00000300255
  gene symbol: EVA1C
  hgvsc: ENST00000300255.2:c.889G>T
  hgvsp: ENSP00000300255.2:p.Val297Phe
  variant of: http://identifiers.org/hgnc/13239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166979
  ensembl protein: ENSP00000372146
  ensembl transcript: ENST00000382699
  gene symbol: EVA1C
  hgvsc: ENST00000382699.3:c.880G>T
  hgvsp: ENSP00000372146.3:p.Val294Phe
  variant of: http://identifiers.org/hgnc/13239
canonical: true
consequence: missense
filter: PASS
hgvs: p.Val297Phe
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 608
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1214
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 333
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3593
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4581
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 348
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1940
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3623
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3241
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2511
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 787
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7819
bin: 9.75e1
variant carriers: 1290

GenotypeQuality
all individuals: 5711
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2776
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 10423
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2476
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1689
bin: 9.25e1
variant carriers: 4

African
type: Population
allele count: 488
allele frequency: 4.746158334954289e-2
allele num: 10282
num of homozygotes: 14

South Asian
type: Population
allele count: 11
allele frequency: 7.842578069299871e-4
allele num: 14026
num of homozygotes: 0

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

East Asian
type: Population
allele count: 254
allele frequency: 2.971455311183903e-2
allele num: 8548
num of homozygotes: 5

Latino
type: Population
allele count: 602
allele frequency: 5.303030303030303e-2
allele num: 11352
num of homozygotes: 18

Other
type: Population
allele count: 3
allele frequency: 3.416856492027335e-3
allele num: 878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.063537773420746e-4
allele num: 65284
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.74e-2

QD
type: SiteQuality
SIO_000300: 1.293e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.680687e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.546e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

GenotypeQuality
all individuals: 2933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3912
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2776
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2476
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4581
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3623
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7819
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1940
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531768886710373e-5
allele num: 65284
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.74e-2

QD
type: SiteQuality
SIO_000300: 1.293e1

FS
type: SiteQuality
SIO_000300: 8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.680687e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.546e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

GenotypeQuality
all individuals: 500
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4495
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23363
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4402
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8838
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.656287266463495e-5
allele num: 60376
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.01e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.246e0

QD
type: SiteQuality
SIO_000300: 1.288e1

VQSLOD
type: SiteQuality
SIO_000300: -2.346e0

DP
type: SiteQuality
SIO_000300: 1.299891e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

GenotypeQuality
all individuals: 377
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41332
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 915
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.144613774609196e-4
allele num: 61156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11144
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 2.235136343316942e-4
allele num: 8948
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.247972045426183e-4
allele num: 16026
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.155e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.282e0

VQSLOD
type: SiteQuality
SIO_000300: -1.211e0

DP
type: SiteQuality
SIO_000300: 1.420274e6

MQRankSum
type: SiteQuality
SIO_000300: -4.74e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

FS
type: SiteQuality
SIO_000300: 9.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeQuality
all individuals: 1072
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 880
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42305
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 1.113833815994654e-4
allele num: 8978
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.231306081754735e-5
allele num: 16048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.630310737226516e-5
allele num: 61338
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.792757260666906e-4
allele num: 11156
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.73134328358209e-4
allele num: 8040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

VQSLOD
type: SiteQuality
SIO_000300: -1.061e0

MQ
type: SiteQuality
SIO_000300: 5.171e1

FS
type: SiteQuality
SIO_000300: 2.666e0

MQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

DP
type: SiteQuality
SIO_000300: 1.432482e6

GenotypeQuality
all individuals: 326
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46036
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4600
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2194
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.16370808678501e-5
allele num: 16224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.756e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.37e-1

DP
type: SiteQuality
SIO_000300: 1.469566e6

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.093e0

MQ
type: SiteQuality
SIO_000300: 5.191e1

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2194
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588966218578193e-5
allele num: 62934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8248
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

FS
type: SiteQuality
SIO_000300: 2.937e0

DP
type: SiteQuality
SIO_000300: 1.476522e6

VQSLOD
type: SiteQuality
SIO_000300: -1.402e0

MQ
type: SiteQuality
SIO_000300: 5.03e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47207
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.206563706563707e-4
allele num: 8288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63542
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 2.376e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 1.0009e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.446e0

VQSLOD
type: SiteQuality
SIO_000300: -2.384e0

DP
type: SiteQuality
SIO_000300: 1.491268e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.64e-1

MQ
type: SiteQuality
SIO_000300: 5.162e1

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
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GenotypeQuality
all individuals: 453
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.541307028360049e-4
allele num: 6488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63642
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.16e-1

QD
type: SiteQuality
SIO_000300: 9.49e0

VQSLOD
type: SiteQuality
SIO_000300: -1.505e0

MQRankSum
type: SiteQuality
SIO_000300: -1.227e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

DP
type: SiteQuality
SIO_000300: 1.49261e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.992e0

MQ
type: SiteQuality
SIO_000300: 5.03e1

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 944
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variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.518648838845883e-4
allele num: 11368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9396
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64048
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.501417e6

MQRankSum
type: SiteQuality
SIO_000300: 6.98e-1

FS
type: SiteQuality
SIO_000300: 5.348e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

MQ
type: SiteQuality
SIO_000300: 4.967e1

VQSLOD
type: SiteQuality
SIO_000300: -1.694e0

QD
type: SiteQuality
SIO_000300: 1.015e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 2194
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 831
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variant carriers: 0

GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 243
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.796622097114708e-5
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64056
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

MQ
type: SiteQuality
SIO_000300: 4.607e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.126e0

DP
type: SiteQuality
SIO_000300: 1.502232e6

FS
type: SiteQuality
SIO_000300: 7.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

GenotypeQuality
all individuals: 927
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 48463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 2194
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variant carriers: 1

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 959
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variant carriers: 0

GenotypeQuality
all individuals: 4771
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variant carriers: 0

GenotypeQuality
all individuals: 461
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.784258608573436e-5
allele num: 11384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64220
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.892e1

DP
type: SiteQuality
SIO_000300: 1.505727e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.093e0

VQSLOD
type: SiteQuality
SIO_000300: -1.955e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.243e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4783
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64258
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.054407423028258e-4
allele num: 9484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.359e0

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.541e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.106e1

QD
type: SiteQuality
SIO_000300: 1.692e1

DP
type: SiteQuality
SIO_000300: 1.506067e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.035e0

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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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55574224462491e-5
allele num: 64278
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.143e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

DP
type: SiteQuality
SIO_000300: 1.506242e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.648e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.721e0

QD
type: SiteQuality
SIO_000300: 1.426e1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-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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bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 4792
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GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.781173164734808e-5
allele num: 11388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9490
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.506501397496658e-4
allele num: 16458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.219e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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QD
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DP
type: SiteQuality
SIO_000300: 1.50714e6

ClippingRankSum
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SIO_000300: 2.97e-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
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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MQ
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FS
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DP
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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QD
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele num: 11388
num of homozygotes: 0

South Asian
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European (Finnish)
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East Asian
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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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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variant carriers: 0

European (Non-Finnish)
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allele frequency: 6.218712104723112e-5
allele num: 64322
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Latino
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele num: 16456
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European (Finnish)
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num of homozygotes: 0

Other
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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South Asian
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Latino
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Other
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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African
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Other
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South Asian
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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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.776775437832457e-5
allele num: 64294
num of homozygotes: 0

MQ
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SIO_000300: 4.78e1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 1.2e0

BaseQRankSum
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SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 5.493e0

DP
type: SiteQuality
SIO_000300: 1.506261e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.564210855623338e-5
allele num: 63930
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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QD
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: 1.5e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.075268817204301e-4
allele num: 9300
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 63776
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQ
type: SiteQuality
SIO_000300: 4.577e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 62620
num of homozygotes: 0

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

Other
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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: 1
allele frequency: 6.187353050365054e-5
allele num: 16162
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9094
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8232
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

DP
type: SiteQuality
SIO_000300: 1.466063e6

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.828e1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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ClippingRankSum
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SIO_000300: -3.2e-2

VQSLOD
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FS
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.237776952593143e-4
allele num: 16158
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.596882884609243e-5
allele num: 62622
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

FS
type: SiteQuality
SIO_000300: 8.815e0

DP
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MQ
type: SiteQuality
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.34e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.632386549134835e-5
allele num: 61260
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.123090745732255e-4
allele num: 8904
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Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
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ClippingRankSum
type: SiteQuality
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DP
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MQRankSum
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VQSLOD
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
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QD
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BaseQRankSum
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SIO_000300: -6.59e-1

InbreedingCoeff
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SIO_000300: -1.5e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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num of homozygotes: 0

East Asian
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allele frequency: 1.299376299376299e-4
allele num: 7696
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 8614
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
type: Population
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MQ
type: SiteQuality
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BaseQRankSum
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MQRankSum
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SIO_000300: -4.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.203e0

DP
type: SiteQuality
SIO_000300: 1.347971e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

FS
type: SiteQuality
SIO_000300: 7.786e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.75e-1

QD
type: SiteQuality
SIO_000300: 5.89e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58494
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10582
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.402048655569782e-5
allele num: 15620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7592
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 5.89e0

MQ
type: SiteQuality
SIO_000300: 3.779e1

DP
type: SiteQuality
SIO_000300: 1.347971e6

FS
type: SiteQuality
SIO_000300: 7.786e0

MQRankSum
type: SiteQuality
SIO_000300: -4.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.203e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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: 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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.740886459385119e-5
allele num: 57442
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6204
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.307123e6

QD
type: SiteQuality
SIO_000300: 1.037e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

MQ
type: SiteQuality
SIO_000300: 3.709e1

VQSLOD
type: SiteQuality
SIO_000300: -2.931e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.228458109578463e-4
allele num: 56982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15412
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

FS
type: SiteQuality
SIO_000300: 1.381e0

VQSLOD
type: SiteQuality
SIO_000300: -2.943e0

MQ
type: SiteQuality
SIO_000300: 3.691e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 1.003e1

DP
type: SiteQuality
SIO_000300: 1.292411e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

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: 3

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.980720982437607e-4
allele num: 15146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7174
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55254
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.846e1

FS
type: SiteQuality
SIO_000300: 8.65e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.081e0

DP
type: SiteQuality
SIO_000300: 1.220477e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

QD
type: SiteQuality
SIO_000300: 1.016e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2964
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.646903820816864e-4
allele num: 6072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQ
type: SiteQuality
SIO_000300: 3.731e1

VQSLOD
type: SiteQuality
SIO_000300: -3.089e0

DP
type: SiteQuality
SIO_000300: 1.211256e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 5.885e0

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15050
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.65724317009838e-5
allele num: 54686
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.195974e6

MQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

FS
type: SiteQuality
SIO_000300: 1.6194e1

MQ
type: SiteQuality
SIO_000300: 3.738e1

QD
type: SiteQuality
SIO_000300: 1.2e1

VQSLOD
type: SiteQuality
SIO_000300: -4.328e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.755304367418979e-5
allele num: 53258
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.551e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.04e-1

MQ
type: SiteQuality
SIO_000300: 4.621e1

FS
type: SiteQuality
SIO_000300: 1.1964e1

DP
type: SiteQuality
SIO_000300: 1.11762e6

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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.041666666666667e-4
allele num: 9600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52464
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6804
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5914
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14638
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.12e-1

ClippingRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 7.207e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -4.1e-3

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.918e1

GenotypeQuality
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GenotypeQuality
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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: 1876
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4544
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.929012345679012e-5
allele num: 51840
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -2.912e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

DP
type: SiteQuality
SIO_000300: 1.051351e6

MQ
type: SiteQuality
SIO_000300: 4.056e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.074e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16501
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10648
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506477854775535e-4
allele num: 6638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51190
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: -2.077e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.035046e6

MQ
type: SiteQuality
SIO_000300: 4.488e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

GenotypeQuality
all individuals: 519
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1650
bin: 6.75e1
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GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9332
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506931886678722e-4
allele num: 6636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50934
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.028802e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.838e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.658e0

MQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.33e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

GenotypeQuality
all individuals: 3025
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4836
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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
all individuals: 7961
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.527650473571647e-4
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14302
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.978e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.615e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 1.005638e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

GenotypeQuality
all individuals: 1055
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 164
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 17247
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2271
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1427
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 472
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variant carriers: 4

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4836
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6039
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 7961
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3025
bin: 9.75e1
variant carriers: 874

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 465
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 10339
bin: 6.25e1
variant carriers: 8

East Asian
type: Population
allele count: 315
allele frequency: 4.812098991750687e-2
allele num: 6546
num of homozygotes: 9

Latino
type: Population
allele count: 552
allele frequency: 6.048652202498356e-2
allele num: 9126
num of homozygotes: 14

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.381519409383186e-4
allele num: 50388
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 1.04880436302615e-3
allele num: 14302
num of homozygotes: 0

African
type: Population
allele count: 27
allele frequency: 3.543307086614173e-3
allele num: 7620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

DP
type: SiteQuality
SIO_000300: 1.005638e6

MQ
type: SiteQuality
SIO_000300: 4.978e1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

QD
type: SiteQuality
SIO_000300: 1.615e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

GenotypeQuality
all individuals: 388
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
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variant carriers: 0

GenotypeQuality
all individuals: 296
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variant carriers: 0

GenotypeQuality
all individuals: 1199
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variant carriers: 0

GenotypeQuality
all individuals: 1596
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variant carriers: 0

GenotypeQuality
all individuals: 2684
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variant carriers: 0

GenotypeQuality
all individuals: 414
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GenotypeQuality
all individuals: 2108
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variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 213
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variant carriers: 0

GenotypeQuality
all individuals: 6222
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variant carriers: 0

GenotypeQuality
all individuals: 6000
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8619
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.020120399175791e-5
allele num: 49502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

MQ
type: SiteQuality
SIO_000300: 5.253e1

MQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.084e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.88e0

DP
type: SiteQuality
SIO_000300: 9.74814e5

GenotypeQuality
all individuals: 1359
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6012
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
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variant carriers: 0

GenotypeQuality
all individuals: 2389
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GenotypeQuality
all individuals: 213
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variant carriers: 0

GenotypeQuality
all individuals: 6232
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
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GenotypeQuality
all individuals: 323
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GenotypeQuality
all individuals: 840
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variant carriers: 0

GenotypeQuality
all individuals: 162
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variant carriers: 0

GenotypeQuality
all individuals: 410
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GenotypeQuality
all individuals: 6124
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variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8637
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: -7.685999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 9.72804e5

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.798e1

MQ
type: SiteQuality
SIO_000300: 5.346e1

GenotypeQuality
all individuals: 2715
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6232
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14030
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.025603629881705e-5
allele num: 49368
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

DP
type: SiteQuality
SIO_000300: 9.72804e5

VQSLOD
type: SiteQuality
SIO_000300: -7.685999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 1.798e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 5.346e1

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6120
bin: 3.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
all individuals: 14754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4529
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1496
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.195279896387969e-5
allele num: 13898
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.796e0

VQSLOD
type: SiteQuality
SIO_000300: -3.487e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.591e0

QD
type: SiteQuality
SIO_000300: 3.14e0

MQRankSum
type: SiteQuality
SIO_000300: -1.874e0

DP
type: SiteQuality
SIO_000300: 9.64378e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

MQ
type: SiteQuality
SIO_000300: 5.284e1

GenotypeQuality
all individuals: 568
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36948
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512081531436175e-5
allele num: 66134
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14538
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: 8642
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.344e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.905035e6

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.194e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.948e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 105

GenotypeQuality
all individuals: 361
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variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 6
allele frequency: 5.189413596263622e-4
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 99
allele frequency: 9.552296410652257e-3
allele num: 10364
num of homozygotes: 2

Other
type: Population
allele count: 2
allele frequency: 2.262443438914027e-3
allele num: 884
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66086
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: 5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 2.905095e6

QD
type: SiteQuality
SIO_000300: 1.555e1

GenotypeQuality
all individuals: 2890
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
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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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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: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4567
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
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: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.377220768489189e-4
allele num: 14522
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.654e1

FS
type: SiteQuality
SIO_000300: 3.711e0

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.632e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

MQ
type: SiteQuality
SIO_000300: 5.9e1

DP
type: SiteQuality
SIO_000300: 2.90278e6

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 525
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variant carriers: 0

GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 1091
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variant carriers: 0

GenotypeQuality
all individuals: 1671
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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: 97
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variant carriers: 0

GenotypeQuality
all individuals: 4631
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variant carriers: 0

GenotypeQuality
all individuals: 277
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variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 14562
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: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.019e0

QD
type: SiteQuality
SIO_000300: 1.424e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 2.902907e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: -1.039e-1

GenotypeQuality
all individuals: 2893
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
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GenotypeQuality
all individuals: 548
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GenotypeQuality
all individuals: 1271
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variant carriers: 0

GenotypeQuality
all individuals: 285
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 935
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 6.75e1
variant carriers: 0

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: 6614
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: 0
allele frequency: 0.0e0
allele num: 66140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14592
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.147e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.09e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.17e-1

FS
type: SiteQuality
SIO_000300: 1.1256e1

DP
type: SiteQuality
SIO_000300: 2.907472e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.904e0

VQSLOD
type: SiteQuality
SIO_000300: -1.242e0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
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variant carriers: 0

GenotypeQuality
all individuals: 539
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variant carriers: 0

GenotypeQuality
all individuals: 92
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 36910
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 270
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 731
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 14682
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511076188461422e-5
allele num: 66178
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.777e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.45e-1

MQ
type: SiteQuality
SIO_000300: 4.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.908073e6

QD
type: SiteQuality
SIO_000300: 1.97e1

GenotypeQuality
all individuals: 1205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.5e0
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 5464
bin: 6.25e1
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GenotypeQuality
all individuals: 1273
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 716
bin: 3.75e1
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GenotypeQuality
all individuals: 36909
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 252
bin: 4.75e1
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GenotypeQuality
all individuals: 535
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variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5109391998066e-5
allele num: 66184
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14684
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.733e0

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

DP
type: SiteQuality
SIO_000300: 2.908906e6

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.655e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

QD
type: SiteQuality
SIO_000300: 1.395e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.25e1
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GenotypeQuality
all individuals: 2891
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1173
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 5659
bin: 6.25e1
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 2521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36909
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 219
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 6.779661016949152e-5
allele num: 14750
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66200
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.011e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.911095e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

MQRankSum
type: SiteQuality
SIO_000300: -2.326e0

FS
type: SiteQuality
SIO_000300: 8.222e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

QD
type: SiteQuality
SIO_000300: 1.563e1

MQ
type: SiteQuality
SIO_000300: 5.693e1

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 888
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 5
allele frequency: 7.559721802237678e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510437120502674e-5
allele num: 66206
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QD
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FS
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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ClippingRankSum
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SIO_000300: -4.03e-1

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.508386629660915e-5
allele num: 66296
num of homozygotes: 0

ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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DP
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66296
num of homozygotes: 0

South Asian
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allele num: 15128
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
type: SiteQuality
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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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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15612
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.342e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

QD
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.938811e6

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.0e-3

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

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

European (Finnish)
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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: 8652
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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VQSLOD
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BaseQRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 4.319e0

InbreedingCoeff
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SIO_000300: 1.0e-3

ReadPosRankSum
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.44e-1

MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 262
allele frequency: 2.518262206843522e-2
allele num: 10404
num of homozygotes: 4

South Asian
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allele frequency: 4.936443292607676e-3
allele num: 16206
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East Asian
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allele num: 8654
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European (Non-Finnish)
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allele count: 456
allele frequency: 6.847669389716483e-3
allele num: 66592
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European (Finnish)
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allele count: 5
allele frequency: 7.559721802237678e-4
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 38
allele frequency: 3.28208671618587e-3
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num of homozygotes: 0

Other
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allele frequency: 7.72626931567329e-3
allele num: 906
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 906
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European (Finnish)
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South Asian
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allele num: 16240
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Latino
type: Population
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African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.297e0

FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.29e0

MQ
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SIO_000300: 5.95e1

DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 36695
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1344
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
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: 16352
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.933625e6

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.088e0

FS
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.101e0

QD
type: SiteQuality
SIO_000300: 1.228e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2933
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 6.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.00147072065312e-4
allele num: 66634
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.729475100942127e-4
allele num: 16346
num of homozygotes: 0

African
type: Population
allele count: 202
allele frequency: 1.941187776282914e-2
allele num: 10406
num of homozygotes: 1

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

Latino
type: Population
allele count: 618
allele frequency: 5.338631651693158e-2
allele num: 11576
num of homozygotes: 21

East Asian
type: Population
allele count: 397
allele frequency: 4.587474000462214e-2
allele num: 8654
num of homozygotes: 10

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

MQ
type: SiteQuality
SIO_000300: 5.909e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 7.72e-1

DP
type: SiteQuality
SIO_000300: 3.039083e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.418e0

QD
type: SiteQuality
SIO_000300: 1.279e1

GenotypeQuality
all individuals: 1743
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36279
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 2625
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9308
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2821
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.831725485407254e-4
allele num: 16378
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.726888333653661e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.882e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

FS
type: SiteQuality
SIO_000300: 1.111e0

VQSLOD
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

DP
type: SiteQuality
SIO_000300: 2.8985e6

GenotypeQuality
all individuals: 2624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3003
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1371
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3372
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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: 11578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

VQSLOD
type: SiteQuality
SIO_000300: -5.517e-1

FS
type: SiteQuality
SIO_000300: 6.74e0

MQ
type: SiteQuality
SIO_000300: 5.792e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

DP
type: SiteQuality
SIO_000300: 2.8979e6

MQRankSum
type: SiteQuality
SIO_000300: -1.047e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.4e-2

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36278
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 9362
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1743
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3372
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3004
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 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: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.497e0

FS
type: SiteQuality
SIO_000300: 4.037e0

QD
type: SiteQuality
SIO_000300: 1.208e1

MQ
type: SiteQuality
SIO_000300: 5.865e1

VQSLOD
type: SiteQuality
SIO_000300: -8.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

DP
type: SiteQuality
SIO_000300: 2.898556e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1