21-34948854-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948854
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948854
    reference: chr 21
allele count: 1
allele frequency: 1.496199652881681e-5
allele num: 66836
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*124C>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1751G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.4336C>G
  hgvsp: ENSP00000400985.1:p.Thr1446Ser
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*124C>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.624C>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*454C>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-740G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*507C>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.561C>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.582C>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.885C>G
  variant of: http://identifiers.org/hgnc/11183
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr1446Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

21-34948866-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948866
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948866
    reference: chr 21
allele count: 1
allele frequency: 1.6679454248257e-5
allele num: 59954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*466G>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1739C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-752C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*136G>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.4348G>T
  hgvsp: ENSP00000400985.1:p.Ser1450Ile
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.636G>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*519G>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*136G>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.897G>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.573G>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.594G>T
  variant of: http://identifiers.org/hgnc/11183
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15722
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9096
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser1450Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

21-34948899-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948899
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948899
    reference: chr 21
allele count: 1
allele frequency: 3.503117774819589e-5
allele num: 28546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*169A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.669A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*169A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*17A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1706T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-785T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*552A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.606A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*499A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.930A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.627A>G
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11925
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

21-34948901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948901
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948901
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 27738
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*171T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.671T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.932T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*554T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*501T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-787A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*171T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.608T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*19T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1704A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.629T>C
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

21-34948903-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948903
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948903
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 26268
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*173A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.610A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1702T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-789T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*503A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.673A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*556A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*21A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.934A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*173A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.631A>G
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11479
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum

21-34948904-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948904
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948904
    reference: chr 21
allele count: 1
allele frequency: 3.875968992248062e-5
allele num: 25800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.611T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-790A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1701A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*504T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*22T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*174T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*557T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.674T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.935T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*174T>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.632T>C
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

21-34948909-G-GAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948909
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948911
    reference: chr 21
allele count: 6
allele frequency: 2.402883460152183e-4
allele num: 24970
alternate allele: GAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.638_639insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*28_*29insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1695_*8+1696insAT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*180_*181insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*563_*564insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*510_*511insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*180_*181insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.617_618insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-796_*9-795insAT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.680_681insTA
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.941_942insTA
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-34948910-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948910
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948910
    reference: chr 21
allele count: 1
allele frequency: 4.027710649266957e-5
allele num: 24828
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*180A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*180A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-796T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*510A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1695T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*563A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.941A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.638A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.617A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*28A>C
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.680A>C
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28076
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum

21-34948925-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948925
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948925
    reference: chr 21
allele count: 7
allele frequency: 3.164556962025317e-4
allele num: 22120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*43C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*195C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-811G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1680G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*525C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.956C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*195C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*578C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.653C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.695C>T
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.632C>T
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29358
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10280
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

21-34948928-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34948928
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34948928
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 21856
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000348984
  ensembl transcript: ENST00000356577
  gene symbol: SON
  hgvsc: ENST00000356577.4:c.*198A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000290239
  ensembl transcript: ENST00000290239
  gene symbol: SON
  hgvsc: ENST00000290239.6:c.*581A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000491794
  gene symbol: SON
  hgvsc: ENST00000491794.1:n.635A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*9-814T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000371111
  ensembl transcript: ENST00000381692
  gene symbol: SON
  hgvsc: ENST00000381692.2:c.*198A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000400985
  ensembl transcript: ENST00000436227
  gene symbol: SON
  hgvsc: ENST00000436227.1:c.*46A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+1677T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000470533
  gene symbol: SON
  hgvsc: ENST00000470533.1:n.656A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000465834
  gene symbol: SON
  hgvsc: ENST00000465834.1:n.698A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159140
  ensembl protein: ENSP00000399783
  ensembl transcript: ENST00000455528
  gene symbol: SON
  hgvsc: ENST00000455528.1:c.*528A>G
  variant of: http://identifiers.org/hgnc/11183
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159140
  ensembl transcript: ENST00000478183
  gene symbol: SON
  hgvsc: ENST00000478183.1:n.959A>G
  variant of: http://identifiers.org/hgnc/11183
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29265
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

21-34950566-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950566
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950566
    reference: chr 21
allele count: 122
allele frequency: 1.018636029657337e-3
allele num: 119768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*777A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+39A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*1037A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*76A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*385A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*47A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*47A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*8+39A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.450A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*47A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*936A>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 13167
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12223
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 3.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

21-34950567-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950567
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950567
    reference: chr 21
allele count: 1
allele frequency: 8.354358468813179e-6
allele num: 119698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*776T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*75T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*384T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*46T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*46T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*935T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*1036T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*8+38T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.449T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+38T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*46T>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13239
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-34950569-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950569
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950569
    reference: chr 21
allele count: 1
allele frequency: 8.344877079960612e-6
allele num: 119834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*73T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*44T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*933T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+36T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*8+36T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*382T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*44T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*774T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*1034T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*44T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.447T>A
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

21-34950573-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950573
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950574
    reference: chr 21
allele count: 1
allele frequency: 8.355056480181806e-6
allele num: 119688
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*769dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*68dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*39dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*928dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+31dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*377dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.442dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*39dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*1029dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*39dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*8+31dupA
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/21-34950583-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950583
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950584
    reference: chr 21
allele count: 1
allele frequency: 8.327504080476999e-6
allele num: 120084
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*1019dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*58dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*759dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.432dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*29dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+21dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*29dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*918dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*367dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*29dupT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*8+21dupT
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/21-34950583-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950583
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950581
    reference: chr 21
allele count: 1
allele frequency: 8.327504080476999e-6
allele num: 120084
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*28_*29delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*366_*367delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*28_*29delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*57_*58delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+20_*8+21delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*917_*918delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*28_*29delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*8+20_*8+21delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.431_432delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*1018_*1019delTT
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*758_*759delTT
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12376
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: CAA
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

21-34950603-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950603
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950603
    reference: chr 21
allele count: 2
allele frequency: 1.654670306941342e-5
allele num: 120870
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*10T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*10T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*8+2T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.413T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*740T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*8+2T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*1000T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*39T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*348T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*899T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*10T>C
  variant of: http://identifiers.org/hgnc/2993
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8596
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8186
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*8+2T>C
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

21-34950609-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950609
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950609
    reference: chr 21
allele count: 910
allele frequency: 7.520412548345509e-3
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*342C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*994C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*4C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.407C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*4C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*893C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*734C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 8591
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 4.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 12317
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 9.75e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 62
genotype quality: GenotypeQuality
num of homozygotes: 9
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

21-34950609-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950609
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950609
    reference: chr 21
allele count: 3
allele frequency: 2.479256884069948e-5
allele num: 121004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.*4C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*994C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.407C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.*4C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.*4C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*33C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*893C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.*4C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*734C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.*4C>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*342C>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

21-34950617-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950617
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950617
    reference: chr 21
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.53C>A
  hgvsp: ENSP00000476496.1:p.Ser18Tyr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1484C>A
  hgvsp: ENSP00000398329.1:p.Ser495Tyr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.399C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1697C>A
  hgvsp: ENSP00000307143.4:p.Ser566Tyr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1609C>A
  hgvsp: ENSP00000399535.1:p.Ser537Tyr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*25C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*726C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*986C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*334C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*885C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1655C>A
  hgvsp: ENSP00000304716.3:p.Ser552Tyr
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser566Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

21-34950638-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950638
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950638
    reference: chr 21
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1676A>C
  hgvsp: ENSP00000307143.4:p.Asp559Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.*4A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1634A>C
  hgvsp: ENSP00000304716.3:p.Asp545Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*313A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1463A>C
  hgvsp: ENSP00000398329.1:p.Asp488Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.378A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*864A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.32A>C
  hgvsp: ENSP00000476496.1:p.Asp11Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1588A>C
  hgvsp: ENSP00000399535.1:p.Asp530Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*705A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*965A>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12539
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp559Ala
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: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

21-34950643-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950643
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950643
    reference: chr 21
allele count: 11
allele frequency: 9.065435965056865e-5
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1458G>A
  hgvsp: ENST00000432378.1:c.1458G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.27G>A
  hgvsp: ENST00000439593.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*960G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1583G>A
  hgvsp: ENST00000437395.1:c.1583G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1629G>A
  hgvsp: ENST00000303113.6:c.1629G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*700G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*859G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.373G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*308G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1671G>A
  hgvsp: ENST00000303071.5:c.1671G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1526G>A
  hgvsp: ENST00000453626.1:c.1526G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
canonical: false
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 14818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter509Ter
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/21-34950644-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950644
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950644
    reference: chr 21
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*959T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1457T>G
  hgvsp: ENSP00000398329.1:p.Leu486Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1525T>G
  hgvsp: ENSP00000394276.1:p.Ter509GlyextTer20
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*858T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*307T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.26T>G
  hgvsp: ENSP00000476496.1:p.Leu9Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1670T>G
  hgvsp: ENSP00000307143.4:p.Leu557Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1582T>G
  hgvsp: ENSP00000399535.1:p.Leu528Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*699T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1628T>G
  hgvsp: ENSP00000304716.3:p.Leu543Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.372T>G
  variant of: http://identifiers.org/hgnc/2993
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter509GlyextTer20
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

21-34950655-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950655
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950655
    reference: chr 21
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.15G>C
  hgvsp: ENST00000439593.1:c.15G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*688G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.361G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1514G>C
  hgvsp: ENSP00000394276.1:p.Gly505Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1659G>C
  hgvsp: ENST00000303071.5:c.1659G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1617G>C
  hgvsp: ENST00000303113.6:c.1617G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*948G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1571G>C
  hgvsp: ENST00000437395.1:c.1571G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1446G>C
  hgvsp: ENST00000432378.1:c.1446G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*847G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*296G>C
  variant of: http://identifiers.org/hgnc/2993
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly505Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

21-34950655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950655
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950655
    reference: chr 21
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*948G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1571G>A
  hgvsp: ENST00000437395.1:c.1571G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1446G>A
  hgvsp: ENST00000432378.1:c.1446G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.361G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1514G>A
  hgvsp: ENSP00000394276.1:p.Gly505Glu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*296G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1617G>A
  hgvsp: ENST00000303113.6:c.1617G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.15G>A
  hgvsp: ENST00000439593.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*688G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1659G>A
  hgvsp: ENST00000303071.5:c.1659G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*847G>A
  variant of: http://identifiers.org/hgnc/2993
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly505Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

21-34950656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950656
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950656
    reference: chr 21
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*846G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*687G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1658G>A
  hgvsp: ENSP00000307143.4:p.Arg553Gln
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1513G>A
  hgvsp: ENSP00000394276.1:p.Gly505Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.360G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*947G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1616G>A
  hgvsp: ENSP00000304716.3:p.Arg539Gln
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*295G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1570G>A
  hgvsp: ENSP00000399535.1:p.Arg524Gln
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1445G>A
  hgvsp: ENSP00000398329.1:p.Arg482Gln
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.14G>A
  hgvsp: ENSP00000476496.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg553Gln
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

21-34950657-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950657
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950657
    reference: chr 21
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*845C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.13C>T
  hgvsp: ENSP00000476496.1:p.Arg5Trp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1615C>T
  hgvsp: ENSP00000304716.3:p.Arg539Trp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.359C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1657C>T
  hgvsp: ENSP00000307143.4:p.Arg553Trp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1444C>T
  hgvsp: ENSP00000398329.1:p.Arg482Trp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*686C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*946C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1569C>T
  hgvsp: ENSP00000399535.1:p.Arg524Trp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1512C>T
  hgvsp: ENST00000453626.1:c.1512C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*294C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg553Trp
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

21-34950658-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950658
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950658
    reference: chr 21
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1656A>T
  hgvsp: ENSP00000307143.4:p.Leu552Phe
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1614A>T
  hgvsp: ENSP00000304716.3:p.Leu538Phe
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.12A>T
  hgvsp: ENSP00000476496.1:p.Leu4Phe
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1568A>T
  hgvsp: ENSP00000399535.1:p.Leu523Phe
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*685A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*844A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.358A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1511A>T
  hgvsp: ENSP00000394276.1:p.Tyr504Phe
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1443A>T
  hgvsp: ENSP00000398329.1:p.Leu481Phe
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*945A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*293A>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu552Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

21-34950665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950665
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950665
    reference: chr 21
allele count: 3
allele frequency: 2.471495419495156e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*938C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000476496
  ensembl transcript: ENST00000439593
  gene symbol: DONSON
  hgvsc: ENST00000439593.1:c.5C>T
  hgvsp: ENSP00000476496.1:p.Ser2Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1607C>T
  hgvsp: ENSP00000304716.3:p.Ser536Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.351C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1504C>T
  hgvsp: ENSP00000394276.1:p.His502Tyr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1436C>T
  hgvsp: ENSP00000398329.1:p.Ser479Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*286C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1561C>T
  hgvsp: ENSP00000399535.1:p.Ser521Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1649C>T
  hgvsp: ENSP00000307143.4:p.Ser550Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*837C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser550Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

21-34950679-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950679
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950679
    reference: chr 21
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*924G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1547G>A
  hgvsp: ENST00000437395.1:c.1547G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*272G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1635G>A
  hgvsp: ENST00000303071.5:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1490G>A
  hgvsp: ENSP00000394276.1:p.Arg497His
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*664G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*823G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1593G>A
  hgvsp: ENST00000303113.6:c.1593G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.337G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1422G>A
  hgvsp: ENST00000432378.1:c.1422G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg497His
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

21-34950680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950680
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950680
    reference: chr 21
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1421C>T
  hgvsp: ENSP00000398329.1:p.Pro474Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1634C>T
  hgvsp: ENSP00000307143.4:p.Pro545Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*923C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1592C>T
  hgvsp: ENSP00000304716.3:p.Pro531Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1489C>T
  hgvsp: ENSP00000394276.1:p.Arg497Cys
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*663C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*271C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*822C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1546C>T
  hgvsp: ENSP00000399535.1:p.Pro516Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.336C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro545Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

21-34950681-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950681
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950681
    reference: chr 21
allele count: 5
allele frequency: 4.118887570844866e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1488C>T
  hgvsp: ENST00000453626.1:c.1488C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1420C>T
  hgvsp: ENSP00000398329.1:p.Pro474Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1633C>T
  hgvsp: ENSP00000307143.4:p.Pro545Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1591C>T
  hgvsp: ENSP00000304716.3:p.Pro531Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*821C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*270C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*922C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1545C>T
  hgvsp: ENSP00000399535.1:p.Pro516Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.335C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*662C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro545Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

21-34950684-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950684
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950684
    reference: chr 21
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*818A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1588A>G
  hgvsp: ENSP00000304716.3:p.Ile530Val
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1417A>G
  hgvsp: ENSP00000398329.1:p.Ile473Val
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1630A>G
  hgvsp: ENSP00000307143.4:p.Ile544Val
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*919A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1485A>G
  hgvsp: ENST00000453626.1:c.1485A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*267A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1542A>G
  hgvsp: ENSP00000399535.1:p.Ile515Val
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.332A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*659A>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile544Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/21-34950689-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950689
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950689
    reference: chr 21
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1480G>T
  hgvsp: ENSP00000394276.1:p.Val494Phe
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*813G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*914G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1537G>T
  hgvsp: ENSP00000399535.1:p.Ser513Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1625G>T
  hgvsp: ENSP00000307143.4:p.Ser542Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1412G>T
  hgvsp: ENSP00000398329.1:p.Ser471Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*654G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1583G>T
  hgvsp: ENSP00000304716.3:p.Ser528Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*262G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.327G>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4974
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser542Ile
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

21-34950699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950699
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950699
    reference: chr 21
allele count: 65
allele frequency: 5.354465624330692e-4
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1615G>A
  hgvsp: ENSP00000307143.4:p.Glu539Lys
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*803G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1573G>A
  hgvsp: ENSP00000304716.3:p.Glu525Lys
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*904G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.317G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1470G>A
  hgvsp: ENSP00000394276.1:p.Trp490Ter
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1402G>A
  hgvsp: ENSP00000398329.1:p.Glu468Lys
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1527G>A
  hgvsp: ENSP00000399535.1:p.Glu510Lys
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*252G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*644G>A
  variant of: http://identifiers.org/hgnc/2993
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 23020
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Trp490Ter
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-34950704-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950704
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950704
    reference: chr 21
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*639C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*798C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*247C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1397C>T
  hgvsp: ENSP00000398329.1:p.Thr466Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.312C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*899C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1522C>T
  hgvsp: ENSP00000399535.1:p.Thr508Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1568C>T
  hgvsp: ENSP00000304716.3:p.Thr523Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1610C>T
  hgvsp: ENSP00000307143.4:p.Thr537Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1465C>T
  hgvsp: ENSP00000394276.1:p.Leu489Phe
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr537Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

21-34950705-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950705
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950705
    reference: chr 21
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1567A>G
  hgvsp: ENSP00000304716.3:p.Thr523Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*246A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*797A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1609A>G
  hgvsp: ENSP00000307143.4:p.Thr537Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1464A>G
  hgvsp: ENST00000453626.1:c.1464A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1396A>G
  hgvsp: ENSP00000398329.1:p.Thr466Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.311A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*638A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1521A>G
  hgvsp: ENSP00000399535.1:p.Thr508Ala
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*898A>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4060
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr537Ala
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

21-34950710-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950710
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950710
    reference: chr 21
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*241C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1391C>T
  hgvsp: ENSP00000398329.1:p.Pro464Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1604C>T
  hgvsp: ENSP00000307143.4:p.Pro535Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*633C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1562C>T
  hgvsp: ENSP00000304716.3:p.Pro521Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*792C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1459C>T
  hgvsp: ENST00000453626.1:c.1459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1516C>T
  hgvsp: ENSP00000399535.1:p.Pro506Leu
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.306C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*893C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12542
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro535Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

21-34950711-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950711
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950711
    reference: chr 21
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.305C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1603C>T
  hgvsp: ENSP00000307143.4:p.Pro535Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1561C>T
  hgvsp: ENSP00000304716.3:p.Pro521Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*791C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1390C>T
  hgvsp: ENSP00000398329.1:p.Pro464Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*632C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*892C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1515C>T
  hgvsp: ENSP00000399535.1:p.Pro506Ser
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*240C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1458C>T
  hgvsp: ENST00000453626.1:c.1458C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2956
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro535Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

21-34950711-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950711
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950711
    reference: chr 21
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1458C>A
  hgvsp: ENST00000453626.1:c.1458C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*892C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1390C>A
  hgvsp: ENSP00000398329.1:p.Pro464Thr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1603C>A
  hgvsp: ENSP00000307143.4:p.Pro535Thr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*240C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1515C>A
  hgvsp: ENSP00000399535.1:p.Pro506Thr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*791C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*632C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1561C>A
  hgvsp: ENSP00000304716.3:p.Pro521Thr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.305C>A
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro535Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

21-34950726-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950726
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950726
    reference: chr 21
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.290A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1443A>G
  hgvsp: ENST00000453626.1:c.1443A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*877A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1546A>G
  hgvsp: ENSP00000304716.3:p.Asn516Asp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1588A>G
  hgvsp: ENSP00000307143.4:p.Asn530Asp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1500A>G
  hgvsp: ENSP00000399535.1:p.Asn501Asp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*617A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1375A>G
  hgvsp: ENSP00000398329.1:p.Asn459Asp
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*225A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*776A>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn530Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

21-34950726-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950726
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950726
    reference: chr 21
allele count: 3
allele frequency: 2.472350876036327e-5
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*776A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1443A>C
  hgvsp: ENST00000453626.1:c.1443A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1546A>C
  hgvsp: ENSP00000304716.3:p.Asn516His
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*617A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*877A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1588A>C
  hgvsp: ENSP00000307143.4:p.Asn530His
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*225A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.290A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1375A>C
  hgvsp: ENSP00000398329.1:p.Asn459His
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1500A>C
  hgvsp: ENSP00000399535.1:p.Asn501His
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn530His
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

21-34950728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950728
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950728
    reference: chr 21
allele count: 361
allele frequency: 2.975405512330213e-3
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*223C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1544C>T
  hgvsp: ENSP00000304716.3:p.Thr515Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1441C>T
  hgvsp: ENST00000453626.1:c.1441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1586C>T
  hgvsp: ENSP00000307143.4:p.Thr529Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1498C>T
  hgvsp: ENSP00000399535.1:p.Thr500Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*875C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*774C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1373C>T
  hgvsp: ENSP00000398329.1:p.Thr458Ile
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*615C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.288C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 9.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 14832
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 8141
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12483
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr529Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

21-34950740-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950740
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950740
    reference: chr 21
allele count: 2
allele frequency: 1.649675014022238e-5
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1574A>G
  hgvsp: ENSP00000307143.4:p.His525Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*762A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1361A>G
  hgvsp: ENSP00000398329.1:p.His454Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.276A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1429A>G
  hgvsp: ENSP00000394276.1:p.Ile477Val
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1486A>G
  hgvsp: ENSP00000399535.1:p.His496Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1532A>G
  hgvsp: ENSP00000304716.3:p.His511Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*211A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*863A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*603A>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His525Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

21-34950751-C-CATATCAAGTACTTTGTCCATTTGCAGGCAGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950751
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950782
    reference: chr 21
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: CATATCAAGTACTTTGTCCATTTGCAGGCAGA
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

21-34950756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950756
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950756
    reference: chr 21
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*853-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*201-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.266-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1419-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*752-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1522-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*593-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1564-6C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1476-6C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5392
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1564-6C>T
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

21-34950759-ATG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950759
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950757
    reference: chr 21
allele count: 2
allele frequency: 1.653329806229747e-5
allele num: 120968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1476-11_1476-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1419-11_1419-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*201-11_*201-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1522-11_1522-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1564-11_1564-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*752-11_*752-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.266-11_266-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*593-11_*593-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-11_1351-10delCA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*853-11_*853-10delCA
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13472
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: ATG
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-34950781-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950781
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950781
    reference: chr 21
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*752-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1522-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*593-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1419-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.266-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1564-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1476-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*853-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-31T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*201-31T>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

21-34950787-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950787
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950787
    reference: chr 21
allele count: 1
allele frequency: 8.301924386072691e-6
allele num: 120454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1476-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*752-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*853-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*201-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1419-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.266-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1564-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*593-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1522-37A>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-37A>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3972
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

21-34950792-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950792
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950793
    reference: chr 21
allele count: 1
allele frequency: 8.317253310266817e-6
allele num: 120232
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1476-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1419-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.266-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1564-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1522-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*853-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*752-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*593-43dupA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*201-43dupA
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11498
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

21-34950792-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34950792
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34950792
    reference: chr 21
allele count: 3
allele frequency: 2.495175993080045e-5
allele num: 120232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1476-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*593-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*752-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1564-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.266-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1419-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*853-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*201-42G>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1522-42G>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13450
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

21-34951609-T-TTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951609
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951611
    reference: chr 21
allele count: 1
allele frequency: 9.001386213476875e-6
allele num: 111094
alternate allele: TTC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+46_*751+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+46_1475+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+46_*592+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-860_1351-859insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+46_*852+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+46_*200+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+46_265+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+46_1563+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+46_1521+47insGA
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+46_1418+47insGA
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7236
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7975
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

21-34951613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951613
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951613
    reference: chr 21
allele count: 1
allele frequency: 9.000414019044876e-6
allele num: 111106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-863C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+43C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+43C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-34951615-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951615
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951615
    reference: chr 21
allele count: 1
allele frequency: 8.997498695362688e-6
allele num: 111142
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+41T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-865T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+41T>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

21-34951619-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951619
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951619
    reference: chr 21
allele count: 1
allele frequency: 8.994423457456377e-6
allele num: 111180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-869A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+37A>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+37A>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2568
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

21-34951619-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951619
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951619
    reference: chr 21
allele count: 1
allele frequency: 8.994423457456377e-6
allele num: 111180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-869A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+37A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+37A>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7953
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

21-34951623-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951623
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951623
    reference: chr 21
allele count: 1
allele frequency: 8.98811770838951e-6
allele num: 111258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-873T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+33T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+33T>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/21-34951627-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951627
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951627
    reference: chr 21
allele count: 1
allele frequency: 8.980368913554968e-6
allele num: 111354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+29T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-877T>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+29T>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7216
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

21-34951627-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951627
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951627
    reference: chr 21
allele count: 1
allele frequency: 8.980368913554968e-6
allele num: 111354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-877T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+29T>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+29T>A
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

21-34951629-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951629
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951629
    reference: chr 21
allele count: 7
allele frequency: 6.283888110883694e-5
allele num: 111396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+27T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-879T>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

21-34951631-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951631
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951631
    reference: chr 21
allele count: 1
allele frequency: 8.966679817797066e-6
allele num: 111524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+25T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-881T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+25T>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

21-34951636-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951636
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951636
    reference: chr 21
allele count: 2
allele frequency: 1.790221808482071e-5
allele num: 111718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-886C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+20C>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+20C>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7984
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28668
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

21-34951646-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951646
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951646
    reference: chr 21
allele count: 1
allele frequency: 8.884150675195451e-6
allele num: 112560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-896C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+10C>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+10C>A
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28933
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7211
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

21-34951649-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951649
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951649
    reference: chr 21
allele count: 2
allele frequency: 1.772452542583172e-5
allele num: 112838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-899A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+7A>G
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+7A>G
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1563+7A>G
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

21-34951651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951651
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951651
    reference: chr 21
allele count: 1
allele frequency: 8.847052162219548e-6
allele num: 113032
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+5G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-901G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+5G>A
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1563+5G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/21-34951655-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951655
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951655
    reference: chr 21
allele count: 1
allele frequency: 8.807158458394984e-6
allele num: 113544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-905G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+1G>T
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+1G>T
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1563+1G>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

21-34951655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951655
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951655
    reference: chr 21
allele count: 1
allele frequency: 8.807158458394984e-6
allele num: 113544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*852+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*751+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.265+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-905G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*592+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1521+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1418+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*200+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1563+1G>A
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1475+1G>A
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1563+1G>A
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

21-34951657-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951657
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951657
    reference: chr 21
allele count: 2
allele frequency: 1.754016698238967e-5
allele num: 114024
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000408788
  ensembl transcript: ENST00000442660
  gene symbol: DONSON
  hgvsc: ENST00000442660.1:c.*591T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000304716
  ensembl transcript: ENST00000303113
  gene symbol: DONSON
  hgvsc: ENST00000303113.6:c.1520T>C
  hgvsp: ENSP00000304716.3:p.Met507Thr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000399535
  ensembl transcript: ENST00000437395
  gene symbol: DONSON
  hgvsc: ENST00000437395.1:c.1474T>C
  hgvsp: ENSP00000399535.1:p.Met492Thr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392405
  ensembl transcript: ENST00000444517
  gene symbol: DONSON
  hgvsc: ENST00000444517.1:c.*199T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000392014
  ensembl transcript: ENST00000417871
  gene symbol: DONSON
  hgvsc: ENST00000417871.1:c.*851T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000415191
  ensembl transcript: ENST00000457359
  gene symbol: DONSON
  hgvsc: ENST00000457359.1:c.*750T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000307143
  ensembl transcript: ENST00000303071
  gene symbol: DONSON
  hgvsc: ENST00000303071.5:c.1562T>C
  hgvsp: ENSP00000307143.4:p.Met521Thr
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1417T>C
  hgvsp: ENSP00000394276.1:p.Trp473Arg
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000159147
  ensembl transcript: ENST00000460557
  gene symbol: DONSON
  hgvsc: ENST00000460557.1:n.264T>C
  variant of: http://identifiers.org/hgnc/2993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000398329
  ensembl transcript: ENST00000432378
  gene symbol: DONSON
  hgvsc: ENST00000432378.1:c.1351-907T>C
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Met521Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

21-34951657-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34951657
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 34951657
    reference: chr 21
allele count: 1
allele frequency: 8.770083491194836e-6
allele num: 114024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000159147
  ensembl protein: ENSP00000394276
  ensembl transcript: ENST00000453626
  gene symbol: DONSON
  hgvsc: ENST00000453626.1:c.1417T>A
  hgvsp: ENSP00000394276.1:p.Trp473Arg
  variant of: http://identifiers.org/hgnc/2993
canonical: true
consequence: missense
filter: PASS
hgvs: p.Met521Lys
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6144
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32316
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 642
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.659574468085106e-4
allele num: 3760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4680
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.543e0

QD
type: SiteQuality
SIO_000300: 1.074e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

FS
type: SiteQuality
SIO_000300: 8.363e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.077e0

MQ
type: SiteQuality
SIO_000300: 5.69e1

DP
type: SiteQuality
SIO_000300: 8.46423e5

GenotypeQuality
all individuals: 9173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9681
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 317
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32111
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3716
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.247596778383996e-5
allele num: 30792
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12012
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

QD
type: SiteQuality
SIO_000300: 8.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: -1.567e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQ
type: SiteQuality
SIO_000300: 5.15e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

DP
type: SiteQuality
SIO_000300: 7.73901e5

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 309
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27769
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5175
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.084598698481562e-4
allele num: 9220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1000
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

MQ
type: SiteQuality
SIO_000300: 5.868e1

DP
type: SiteQuality
SIO_000300: 5.11372e5

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.061e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.39e-2

QD
type: SiteQuality
SIO_000300: 1.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeQuality
all individuals: 308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11076
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2125
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28012
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5044
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 544
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 585
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2220
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 964
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.52e-2

FS
type: SiteQuality
SIO_000300: 2.944e0

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

DP
type: SiteQuality
SIO_000300: 5.02618e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 4.803e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: -8.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4720
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9090
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2046
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.324e-1

QD
type: SiteQuality
SIO_000300: 1.205e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.75e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.395e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.84446e5

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2512
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2673
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28006
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4613
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 532
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8661
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2208
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.123090745732255e-4
allele num: 8904
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.98e-1

MQ
type: SiteQuality
SIO_000300: 5.847e1

VQSLOD
type: SiteQuality
SIO_000300: -2.188e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.079e1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.84e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.72e0

DP
type: SiteQuality
SIO_000300: 4.79828e5

GenotypeQuality
all individuals: 304
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2922
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 311
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 525
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 9.523809523809524e-4
allele num: 2100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 3.883495145631068e-4
allele num: 10300
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1910
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.412e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 4.67241e5

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.797e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.01e-2

QD
type: SiteQuality
SIO_000300: 1.82e0

FS
type: SiteQuality
SIO_000300: 2.163e1

MQ
type: SiteQuality
SIO_000300: 5.395e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
all individuals: 1400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2976
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7953
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 778
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2775
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 557
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.396648044692737e-3
allele num: 716
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.98e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

DP
type: SiteQuality
SIO_000300: 4.63984e5

MQ
type: SiteQuality
SIO_000300: 5.739e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.405e0

QD
type: SiteQuality
SIO_000300: 1.549e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

GenotypeQuality
all individuals: 907
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2300
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3960
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1067
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6596
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24144
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 315
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 487
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2689
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 594
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3999
bin: 1.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.319148936170213e-3
allele num: 752
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.557031064737965e-4
allele num: 8434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQ
type: SiteQuality
SIO_000300: 5.177e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

QD
type: SiteQuality
SIO_000300: 1.286e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.65e-2

DP
type: SiteQuality
SIO_000300: 4.15102e5

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

FS
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 2680
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4105
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7453
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3498
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 938
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 778
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23056
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.395e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.79e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 5.35e0

VQSLOD
type: SiteQuality
SIO_000300: -1.418e0

DP
type: SiteQuality
SIO_000300: 4.11447e5

GenotypeQuality
all individuals: 605
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14084
bin: 9.75e1
variant carriers: 122

GenotypeQuality
all individuals: 4063
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4944
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2989
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17302
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 3.894839337877313e-4
allele num: 10270
num of homozygotes: 0

Latino
type: Population
allele count: 24
allele frequency: 2.080443828016643e-3
allele num: 11536
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.333333333333334e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 90
allele frequency: 1.359064963305246e-3
allele num: 66222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.19065e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.386e1

VQSLOD
type: SiteQuality
SIO_000300: 5.84e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4061
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2995
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17656
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6709
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4944
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2924
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510528382828313e-5
allele num: 66202
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15556
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.191404e6

VQSLOD
type: SiteQuality
SIO_000300: -2.611e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

MQ
type: SiteQuality
SIO_000300: 5.773e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.882e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

GenotypeQuality
all individuals: 460
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2938
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4951
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13990
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509115054931788e-5
allele num: 66264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15600
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

DP
type: SiteQuality
SIO_000300: 2.19507e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.68e-1

GenotypeQuality
all individuals: 463
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 429
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4032
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18600
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13964
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 816
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4915
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15512
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.721952167995334e-5
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66214
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.67e0

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

FS
type: SiteQuality
SIO_000300: 1.2095e1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.201813e6

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13966
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4048
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20390
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66334
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.351626016260163e-5
allele num: 15744
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.213583e6

FS
type: SiteQuality
SIO_000300: 1.724e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.443e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

GenotypeQuality
all individuals: 20390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13966
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 164
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4048
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66334
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.351626016260163e-5
allele num: 15744
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.724e0

DP
type: SiteQuality
SIO_000300: 2.213583e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.443e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

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

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

GenotypeQuality
all individuals: 295
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4954
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4052
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13968
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2990
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6916
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.167509559639817e-5
allele num: 16214
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503081316699233e-5
allele num: 66530
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

DP
type: SiteQuality
SIO_000300: 2.233522e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

QD
type: SiteQuality
SIO_000300: 1.107e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

GenotypeQuality
all individuals: 4901
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22236
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14345
bin: 9.75e1
variant carriers: 901

GenotypeQuality
all individuals: 1952
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3997
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2925
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6869
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 41
allele frequency: 3.541810642709053e-3
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 15
allele frequency: 1.443140273234558e-3
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 772
allele frequency: 1.159542191114182e-2
allele num: 66578
num of homozygotes: 7

European (Finnish)
type: Population
allele count: 47
allele frequency: 7.106138494103417e-3
allele num: 6614
num of homozygotes: 1

Other
type: Population
allele count: 9
allele frequency: 9.977827050997782e-3
allele num: 902
num of homozygotes: 0

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

South Asian
type: Population
allele count: 26
allele frequency: 1.596071209330878e-3
allele num: 16290
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 1.225e0

DP
type: SiteQuality
SIO_000300: 2.26718e6

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.033e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

GenotypeQuality
all individuals: 3997
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4901
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14345
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2925
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22236
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 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: 3
allele frequency: 4.505992970650966e-5
allele num: 66578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.225e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

DP
type: SiteQuality
SIO_000300: 2.26718e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.033e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

GenotypeDepth
all individuals: 1915
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2961
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6991
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13688
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 22747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 2.237118e6

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.59e0

FS
type: SiteQuality
SIO_000300: 5.212e0

QD
type: SiteQuality
SIO_000300: 1.307e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1238
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13689
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22951
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7025
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2964
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1977
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4981
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.372e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e0

QD
type: SiteQuality
SIO_000300: 1.071e1

VQSLOD
type: SiteQuality
SIO_000300: -1.379e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.239856e6

GenotypeDepth
all individuals: 655
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22970
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 13688
bin: 9.75e1
variant carriers: 11

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

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 11
allele frequency: 1.271088513981974e-3
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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.06e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.1e0

FS
type: SiteQuality
SIO_000300: 5.23e-1

DP
type: SiteQuality
SIO_000300: 2.240457e6

GenotypeDepth
all individuals: 655
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4055
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1977
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13679
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2965
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22985
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 906
num of homozygotes: 0

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

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

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: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.779e0

VQSLOD
type: SiteQuality
SIO_000300: 5.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

QD
type: SiteQuality
SIO_000300: 1.149e1

MQRankSum
type: SiteQuality
SIO_000300: 9.89e-1

FS
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 2.239735e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeDepth
all individuals: 655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13681
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4055
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

MQRankSum
type: SiteQuality
SIO_000300: -1.028e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 3.193e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

DP
type: SiteQuality
SIO_000300: 2.240111e6

GenotypeDepth
all individuals: 3370
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13681
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4055
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.028e0

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 3.193e0

DP
type: SiteQuality
SIO_000300: 2.240111e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.263e1

GenotypeDepth
all individuals: 508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23015
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13679
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 7026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4055
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2963
bin: 7.25e1
variant carriers: 0

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

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

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

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

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: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.95e-1

QD
type: SiteQuality
SIO_000300: 1.148e1

DP
type: SiteQuality
SIO_000300: 2.240066e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

FS
type: SiteQuality
SIO_000300: 5.348e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeDepth
all individuals: 1247
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4976
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4056
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7027
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13679
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

FS
type: SiteQuality
SIO_000300: 1.092e0

QD
type: SiteQuality
SIO_000300: 1.257e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 2.24023e6

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

GenotypeDepth
all individuals: 207
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2962
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13676
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7029
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.424e1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 5.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e0

DP
type: SiteQuality
SIO_000300: 2.240185e6

MQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.989e1

GenotypeDepth
all individuals: 1240
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4055
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13677
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7028
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4975
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.391e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.589e0

MQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 2.240376e6

FS
type: SiteQuality
SIO_000300: 2.945e0

VQSLOD
type: SiteQuality
SIO_000300: 9.340000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.106e0

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1975
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13675
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 7.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
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: 11576
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 2.240388e6

QD
type: SiteQuality
SIO_000300: 1.382e1

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23026
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4054
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13673
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.089e1

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

FS
type: SiteQuality
SIO_000300: 4.447e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

DP
type: SiteQuality
SIO_000300: 2.240339e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4054
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2963
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23027
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13679
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1976
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

South Asian
type: Population
allele count: 5
allele frequency: 3.028467595396729e-4
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e-1

DP
type: SiteQuality
SIO_000300: 2.240363e6

FS
type: SiteQuality
SIO_000300: 4.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 8.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7032
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13674
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 4.237e0

DP
type: SiteQuality
SIO_000300: 2.240252e6

VQSLOD
type: SiteQuality
SIO_000300: -2.392e-1

MQ
type: SiteQuality
SIO_000300: 5.902e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7032
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13674
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-1

DP
type: SiteQuality
SIO_000300: 2.240216e6

VQSLOD
type: SiteQuality
SIO_000300: -1.323e-1

FS
type: SiteQuality
SIO_000300: 1.1908e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.012e0

QD
type: SiteQuality
SIO_000300: 1.208e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

MQ
type: SiteQuality
SIO_000300: 5.896e1

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2957
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13691
bin: 9.75e1
variant carriers: 65

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

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

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

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2961
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 42
allele frequency: 4.036908881199538e-3
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648483395276346e-4
allele num: 66728
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 12
allele frequency: 1.036627505183138e-3
allele num: 11576
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

FS
type: SiteQuality
SIO_000300: 1.108e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

QD
type: SiteQuality
SIO_000300: 1.358e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

DP
type: SiteQuality
SIO_000300: 2.243227e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.982e0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7040
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 23029
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2956
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13643
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4061
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
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: 908
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.794e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.285e0

DP
type: SiteQuality
SIO_000300: 2.239693e6

FS
type: SiteQuality
SIO_000300: 1.186e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.788e1

VQSLOD
type: SiteQuality
SIO_000300: -2.498e0

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

GenotypeQuality
all individuals: 23033
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7039
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13642
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2956
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.292e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 2.239717e6

VQSLOD
type: SiteQuality
SIO_000300: -3.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.509e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23023
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4969
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4060
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2957
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13641
bin: 9.75e1
variant carriers: 1

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

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

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

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

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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.016e0

DP
type: SiteQuality
SIO_000300: 2.239504e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

GenotypeQuality
all individuals: 7041
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4967
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13641
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.128e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.808e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 6.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.808e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.57e-1

DP
type: SiteQuality
SIO_000300: 2.239528e6

GenotypeQuality
all individuals: 4967
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2956
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7041
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13641
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.808e1

FS
type: SiteQuality
SIO_000300: 6.95e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

VQSLOD
type: SiteQuality
SIO_000300: -1.808e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.57e-1

DP
type: SiteQuality
SIO_000300: 2.239528e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22983
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4963
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4059
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13638
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7028
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998860433035446e-5
allele num: 66692
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

DP
type: SiteQuality
SIO_000300: 2.238656e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.592e1

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4963
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13638
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22983
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

QD
type: SiteQuality
SIO_000300: 1.592e1

DP
type: SiteQuality
SIO_000300: 2.238656e6

GenotypeQuality
all individuals: 2945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13763
bin: 9.75e1
variant carriers: 361

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22945
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 4948
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2949
bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 19
allele frequency: 1.64161050630724e-3
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 316
allele frequency: 4.738910050688341e-3
allele num: 66682
num of homozygotes: 0

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

South Asian
type: Population
allele count: 11
allele frequency: 6.669900557846228e-4
allele num: 16492
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.736e0

DP
type: SiteQuality
SIO_000300: 2.253616e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

QD
type: SiteQuality
SIO_000300: 1.297e1

GenotypeQuality
all individuals: 4060
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2971
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4965
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13480
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7039
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1963
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.235109e6

FS
type: SiteQuality
SIO_000300: 7.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.35e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.09e-1

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

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7013
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2968
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4942
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1962
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4052
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22676
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13473
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.669e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.261e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.897e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.02e0

FS
type: SiteQuality
SIO_000300: 9.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.896e0

QD
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 2.231725e6

GenotypeQuality
all individuals: 2938
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13472
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22512
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4048
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4935
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
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: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.638e0

QD
type: SiteQuality
SIO_000300: 7.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.228942e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.156e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

MQ
type: SiteQuality
SIO_000300: 5.851e1

GenotypeQuality
all individuals: 6970
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4932
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2963
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22308
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4047
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

DP
type: SiteQuality
SIO_000300: 2.226285e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

FS
type: SiteQuality
SIO_000300: 6.672e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.599e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
all individuals: 2847
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19611
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13465
bin: 9.75e1
variant carriers: 1

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506296318611797e-5
allele num: 66388
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

MQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

FS
type: SiteQuality
SIO_000300: 3.652e0

DP
type: SiteQuality
SIO_000300: 2.19254e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.512e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

QD
type: SiteQuality
SIO_000300: 1.199e1

GenotypeQuality
all individuals: 1704
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2779
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17485
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2953
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6301
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13457
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1939
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4775
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 1
allele frequency: 1.507613447911955e-5
allele num: 66330
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.171875e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

GenotypeQuality
all individuals: 6108
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13450
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3958
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4722
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66264
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

FS
type: SiteQuality
SIO_000300: 6.625e0

DP
type: SiteQuality
SIO_000300: 2.153635e6

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

QD
type: SiteQuality
SIO_000300: 1.046e1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

GenotypeQuality
all individuals: 2945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4722
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3958
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.600104004160167e-4
allele num: 11538
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

DP
type: SiteQuality
SIO_000300: 2.153635e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

FS
type: SiteQuality
SIO_000300: 6.625e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

QD
type: SiteQuality
SIO_000300: 1.046e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

GenotypeQuality
all individuals: 228
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26761
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559965056782728e-5
allele num: 64104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
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: 9334
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.512e1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

MQ
type: SiteQuality
SIO_000300: 6.014e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

DP
type: SiteQuality
SIO_000300: 1.818011e6

GenotypeQuality
all individuals: 27525
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1622
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2570
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 195
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7941
bin: 6.75e1
variant carriers: 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: 9330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559770401796856e-5
allele num: 64112
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.246e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.474e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.821893e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.537e0

GenotypeQuality
all individuals: 2684
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27831
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 130
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7218
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7951
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2575
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559527151367705e-5
allele num: 64122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
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: 8542
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: 9352
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

DP
type: SiteQuality
SIO_000300: 1.823615e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.123e0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7219
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28086
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7953
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559040878051823e-5
allele num: 64142
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

DP
type: SiteQuality
SIO_000300: 1.826732e6

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

QD
type: SiteQuality
SIO_000300: 1.619e1

GenotypeQuality
all individuals: 459
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28086
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7219
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 9.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559040878051823e-5
allele num: 64142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

DP
type: SiteQuality
SIO_000300: 1.826732e6

QD
type: SiteQuality
SIO_000300: 1.619e1

GenotypeQuality
all individuals: 231
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7963
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7217
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64156
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.060670343657191e-4
allele num: 9428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.830002e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

QD
type: SiteQuality
SIO_000300: 1.029e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

FS
type: SiteQuality
SIO_000300: 5.462e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

GenotypeQuality
all individuals: 213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28471
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 3.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

DP
type: SiteQuality
SIO_000300: 1.832945e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

QD
type: SiteQuality
SIO_000300: 1.728e1

GenotypeQuality
all individuals: 7216
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1432
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28471
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557729453548508e-5
allele num: 64196
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 3.31e0

DP
type: SiteQuality
SIO_000300: 1.832945e6

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.728e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
all individuals: 2678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28531
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1362
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2919
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7217
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7966
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64208
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 7
allele frequency: 6.091193873999304e-4
allele num: 11492
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: 10234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

FS
type: SiteQuality
SIO_000300: 1.192e0

DP
type: SiteQuality
SIO_000300: 1.834127e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

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

GenotypeQuality
all individuals: 320
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2563
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7210
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7970
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28581
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1475
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556614053111671e-5
allele num: 64242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.467e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

DP
type: SiteQuality
SIO_000300: 1.835409e6

MQRankSum
type: SiteQuality
SIO_000300: -1.029e0

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.236e0

QD
type: SiteQuality
SIO_000300: 1.345e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3425
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7210
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2680
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3620
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
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: 8552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.110032966349443e-5
allele num: 64308
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.35e-1

DP
type: SiteQuality
SIO_000300: 1.839239e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.301e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.94e-1

GenotypeQuality
all individuals: 435
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3618
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3731
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8001
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550579916888916e-5
allele num: 64492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.263e0

FS
type: SiteQuality
SIO_000300: 7.831e0

DP
type: SiteQuality
SIO_000300: 1.847311e6

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.879e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

QD
type: SiteQuality
SIO_000300: 1.27e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8004
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3720
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7210
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 336
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2682
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.737098344693281e-5
allele num: 10270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10478
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: 1.548706829797119e-5
allele num: 64570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: 7.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e0

DP
type: SiteQuality
SIO_000300: 1.849672e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.534e1

GenotypeQuality
all individuals: 276
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3650
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2682
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8007
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2559
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7210
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
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: 1.54813140539369e-5
allele num: 64594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.851585e6

FS
type: SiteQuality
SIO_000300: 4.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.27e0

MQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

QD
type: SiteQuality
SIO_000300: 1.74e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.353e-1

GenotypeQuality
all individuals: 215
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7209
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3621
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.72762645914397e-5
allele num: 10280
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: 8604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.855962e6

QD
type: SiteQuality
SIO_000300: 1.295e1

FS
type: SiteQuality
SIO_000300: 2.088e0

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.136e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7209
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2683
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 275
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545021939311538e-5
allele num: 64724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.088e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.136e0

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 1.855962e6

GenotypeDepth
all individuals: 589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3426
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8022
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7208
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 29440
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2563
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.718172983479106e-5
allele num: 10290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
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: 8606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541972491210757e-5
allele num: 64852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.128e0

MQRankSum
type: SiteQuality
SIO_000300: -4.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

FS
type: SiteQuality
SIO_000300: 5.06e-1

QD
type: SiteQuality
SIO_000300: 1.06e1

DP
type: SiteQuality
SIO_000300: 1.858451e6