8-72234095-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234095
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234095
    reference: chr 8
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.292C>T
  hgvsp: ENSP00000373394.4:p.Leu98Phe
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-48C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.292C>T
  hgvsp: ENSP00000342626.3:p.Leu98Phe
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.190C>T
  hgvsp: ENSP00000373393.2:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.283C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.193C>T
  hgvsp: ENSP00000373392.3:p.Leu65Phe
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.292C>T
  hgvsp: ENSP00000410176.1:p.Leu98Phe
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.787C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.289C>T
  hgvsp: ENSP00000373395.2:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.289C>T
  hgvsp: ENSP00000303221.7:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu98Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

8-72234100-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234100
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234100
    reference: chr 8
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.284A>G
  hgvsp: ENSP00000303221.7:p.His95Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.287A>G
  hgvsp: ENSP00000410176.1:p.His96Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.782A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.185A>G
  hgvsp: ENSP00000373393.2:p.His62Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.188A>G
  hgvsp: ENSP00000373392.3:p.His63Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.284A>G
  hgvsp: ENSP00000373395.2:p.His95Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.287A>G
  hgvsp: ENSP00000342626.3:p.His96Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.278A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.287A>G
  hgvsp: ENSP00000373394.4:p.His96Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-53A>G
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His96Arg
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-72234103-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234103
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234103
    reference: chr 8
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.185C>T
  hgvsp: ENSP00000373392.3:p.Pro62Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-56C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.779C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.284C>T
  hgvsp: ENSP00000373394.4:p.Pro95Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.284C>T
  hgvsp: ENSP00000410176.1:p.Pro95Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.284C>T
  hgvsp: ENSP00000342626.3:p.Pro95Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.182C>T
  hgvsp: ENSP00000373393.2:p.Pro61Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.281C>T
  hgvsp: ENSP00000373395.2:p.Pro94Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.275C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.281C>T
  hgvsp: ENSP00000303221.7:p.Pro94Leu
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46417
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro95Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

8-72234103-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234103
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234103
    reference: chr 8
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.275C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-56C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.284C>A
  hgvsp: ENSP00000342626.3:p.Pro95Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.182C>A
  hgvsp: ENSP00000373393.2:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.185C>A
  hgvsp: ENSP00000373392.3:p.Pro62Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.284C>A
  hgvsp: ENSP00000410176.1:p.Pro95Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.284C>A
  hgvsp: ENSP00000373394.4:p.Pro95Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.281C>A
  hgvsp: ENSP00000303221.7:p.Pro94Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.281C>A
  hgvsp: ENSP00000373395.2:p.Pro94Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.779C>A
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro95Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-72234121-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234121
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234121
    reference: chr 8
allele count: 4
allele frequency: 3.296685183048445e-5
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-7C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-7C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-74C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-10C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-10C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.761C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-7C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-7C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-10C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-7C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: c.273-7C>T
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-72234124-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234124
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234124
    reference: chr 8
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-10T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-10T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-77T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.758T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-10T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-10T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-10T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-13T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-72234130-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234130
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234130
    reference: chr 8
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-19C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-16C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-16C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-19C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-16C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.752C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-19C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-16C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-16C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-83C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/8-72234132-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234132
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234132
    reference: chr 8
allele count: 3
allele frequency: 2.473370049137618e-5
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-18G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-21G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-21G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-18G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-18G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-21G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-18G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-85G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-18G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.750G>T
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5006
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

8-72234134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234134
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234134
    reference: chr 8
allele count: 2
allele frequency: 1.649185302460584e-5
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-20C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-23C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-20C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-20C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-23C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-87C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.748C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-20C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-20C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-23C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

8-72234139-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234139
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234139
    reference: chr 8
allele count: 2
allele frequency: 1.649593375233005e-5
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-25A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-25A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-25A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.743A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-25A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-92A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-25A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-28A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-28A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-28A>G
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15349
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

8-72234140-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234140
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234140
    reference: chr 8
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.742T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-29T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-29T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-93T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-29T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5007
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

8-72234145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234145
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234145
    reference: chr 8
allele count: 2
allele frequency: 1.650818806127839e-5
allele num: 121152
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-31C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-34C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-34C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-34C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.737C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-31C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-31C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-31C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-31C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-98C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

8-72234153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234153
    reference: chr 8
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-39T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.729T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-39T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-42T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-39T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-42T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-42T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-106T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-39T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-39T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-72234159-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234159
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234159
    reference: chr 8
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-48A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-45A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.723A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-45A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-45A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-48A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-45A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-48A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-45A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-112A>G
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3107
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

8-72234165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234165
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234165
    reference: chr 8
allele count: 1
allele frequency: 8.323483877411729e-6
allele num: 120142
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-51G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-51G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-51G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.717G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-118G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-54G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-51G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-54G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-51G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-54G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

8-72234169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234169
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234169
    reference: chr 8
allele count: 3
allele frequency: 2.503839220137544e-5
allele num: 119816
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-55G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-55G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-55G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.713G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-58G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-58G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-58G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-55G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-55G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-122G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1929
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

8-72234174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234174
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234174
    reference: chr 8
allele count: 8
allele frequency: 6.714000369270021e-5
allele num: 119154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-63G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-63G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-60G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-63G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.708G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-127G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-60G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-60G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-60G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-60G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4737
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32683
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-72234175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234175
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234175
    reference: chr 8
allele count: 1
allele frequency: 8.394754957102802e-6
allele num: 119122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-61C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-64C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.707C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-64C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-61C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-61C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-128C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-61C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-61C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-64C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-72234187-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234187
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234187
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 117520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-76G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-76G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-73G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-73G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.695G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-73G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-76G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-140G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-73G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-73G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

8-72234209-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234209
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234209
    reference: chr 8
allele count: 1
allele frequency: 8.862576882854458e-6
allele num: 112834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-95A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.673A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-95A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-98A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-95A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-98A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-95A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-98A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-95A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-162A>G
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3340
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

8-72234211-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234211
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234211
    reference: chr 8
allele count: 1
allele frequency: 9.046826373308244e-6
allele num: 110536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.671C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.174-97C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.264-97C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.273-97C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.273-97C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.273-164C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.174-100C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.273-97C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.273-100C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.273-100C>G
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10571
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6502
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

8-72234384-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234384
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234384
    reference: chr 8
allele count: 1
allele frequency: 8.396728634523989e-6
allele num: 119094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.272+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.272+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.272+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.263+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.272+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.498T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.173+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.272+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.272+50T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.173+50T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11875
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2556
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

8-72234387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234387
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234387
    reference: chr 8
allele count: 1
allele frequency: 8.399267583866688e-6
allele num: 119058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.173+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.263+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.272+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.272+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.272+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.272+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.495C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.272+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.173+47C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.272+47C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13116
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

8-72234414-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234414
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234414
    reference: chr 8
allele count: 2
allele frequency: 1.66306336271412e-5
allele num: 120260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.263+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.173+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.272+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.272+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.272+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.272+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.272+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.468A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.173+20A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.272+20A>T
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

8-72234435-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234435
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234435
    reference: chr 8
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.262A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.271A>G
  hgvsp: ENSP00000410176.1:p.Asn91Asp
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.271A>G
  hgvsp: ENSP00000373395.2:p.Lys91Glu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.172A>G
  hgvsp: ENSP00000373393.2:p.Lys58Glu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.271A>G
  hgvsp: ENSP00000373394.4:p.Asn91Asp
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.271A>G
  hgvsp: ENSP00000428391.1:p.Asn91Asp
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.271A>G
  hgvsp: ENSP00000342626.3:p.Asn91Asp
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.447A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.271A>G
  hgvsp: ENSP00000303221.7:p.Lys91Glu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.172A>G
  hgvsp: ENSP00000373392.3:p.Asn58Asp
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn91Asp
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

8-72234440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234440
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234440
    reference: chr 8
allele count: 3
allele frequency: 2.485130635033715e-5
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.167C>T
  hgvsp: ENSP00000373393.2:p.Pro56Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.167C>T
  hgvsp: ENSP00000373392.3:p.Pro56Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.266C>T
  hgvsp: ENSP00000373395.2:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.266C>T
  hgvsp: ENSP00000410176.1:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.257C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.442C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.266C>T
  hgvsp: ENSP00000303221.7:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.266C>T
  hgvsp: ENSP00000373394.4:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.266C>T
  hgvsp: ENSP00000428391.1:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.266C>T
  hgvsp: ENSP00000342626.3:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro89Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

8-72234442-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234442
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234442
    reference: chr 8
allele count: 2
allele frequency: 1.656863557286057e-5
allele num: 120710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.264C>T
  hgvsp: ENST00000388743.2:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.264C>T
  hgvsp: ENST00000303824.7:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.165C>T
  hgvsp: ENST00000388741.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.255C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.264C>T
  hgvsp: ENST00000465115.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.165C>T
  hgvsp: ENST00000388740.3:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.264C>T
  hgvsp: ENST00000419131.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.264C>T
  hgvsp: ENST00000388742.4:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.264C>T
  hgvsp: ENST00000340726.3:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.440C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13479
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Tyr88Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

8-72234444-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234444
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234444
    reference: chr 8
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.438T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.262T>C
  hgvsp: ENSP00000342626.3:p.Tyr88His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.262T>C
  hgvsp: ENSP00000410176.1:p.Tyr88His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.262T>C
  hgvsp: ENSP00000373395.2:p.Tyr88His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.262T>C
  hgvsp: ENSP00000428391.1:p.Tyr88His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.262T>C
  hgvsp: ENSP00000373394.4:p.Tyr88His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.262T>C
  hgvsp: ENSP00000303221.7:p.Tyr88His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.163T>C
  hgvsp: ENSP00000373392.3:p.Tyr55His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.163T>C
  hgvsp: ENSP00000373393.2:p.Tyr55His
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.253T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr88His
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: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

8-72234446-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234446
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234446
    reference: chr 8
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.260T>C
  hgvsp: ENSP00000373395.2:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.260T>C
  hgvsp: ENSP00000342626.3:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.260T>C
  hgvsp: ENSP00000428391.1:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.260T>C
  hgvsp: ENSP00000410176.1:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.161T>C
  hgvsp: ENSP00000373393.2:p.Ile54Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.260T>C
  hgvsp: ENSP00000373394.4:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.436T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.161T>C
  hgvsp: ENSP00000373392.3:p.Ile54Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.251T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.260T>C
  hgvsp: ENSP00000303221.7:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28228
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile87Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

8-72234449-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234449
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234449
    reference: chr 8
allele count: 2
allele frequency: 1.656424442199069e-5
allele num: 120742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.158A>G
  hgvsp: ENSP00000373392.3:p.Gln53Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.257A>G
  hgvsp: ENSP00000342626.3:p.Gln86Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.158A>G
  hgvsp: ENSP00000373393.2:p.Gln53Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.257A>G
  hgvsp: ENSP00000410176.1:p.Gln86Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.257A>G
  hgvsp: ENSP00000373395.2:p.Gln86Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.257A>G
  hgvsp: ENSP00000303221.7:p.Gln86Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.433A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.257A>G
  hgvsp: ENSP00000373394.4:p.Gln86Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.257A>G
  hgvsp: ENSP00000428391.1:p.Gln86Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.248A>G
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln86Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-72234458-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234458
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234458
    reference: chr 8
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.248C>G
  hgvsp: ENSP00000342626.3:p.Ser83Cys
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.248C>G
  hgvsp: ENSP00000410176.1:p.Ser83Cys
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.248C>G
  hgvsp: ENSP00000303221.7:p.Ser83Cys
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.248C>G
  hgvsp: ENSP00000373394.4:p.Ser83Cys
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.424C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.149C>G
  hgvsp: ENSP00000373393.2:p.Ser50Cys
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.239C>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.149C>G
  hgvsp: ENSP00000373392.3:p.Ser50Cys
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.248C>G
  hgvsp: ENSP00000373395.2:p.Ser83Cys
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.248C>G
  hgvsp: ENSP00000428391.1:p.Ser83Cys
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser83Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

8-72234460-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234460
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234460
    reference: chr 8
allele count: 1
allele frequency: 8.283768783445716e-6
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.147C>T
  hgvsp: ENST00000388740.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.246C>T
  hgvsp: ENST00000465115.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.246C>T
  hgvsp: ENST00000340726.3:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.147C>T
  hgvsp: ENST00000388741.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.246C>T
  hgvsp: ENST00000388742.4:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.246C>T
  hgvsp: ENST00000303824.7:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.422C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.237C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.246C>T
  hgvsp: ENST00000419131.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.246C>T
  hgvsp: ENST00000388743.2:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe82Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

8-72234461-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234461
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234461
    reference: chr 8
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.421T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.245T>C
  hgvsp: ENSP00000373394.4:p.Phe82Ser
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.236T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.245T>C
  hgvsp: ENSP00000342626.3:p.Phe82Ser
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.245T>C
  hgvsp: ENSP00000410176.1:p.Phe82Ser
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.245T>C
  hgvsp: ENSP00000373395.2:p.Phe82Ser
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.245T>C
  hgvsp: ENSP00000428391.1:p.Phe82Ser
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.146T>C
  hgvsp: ENSP00000373393.2:p.Phe49Ser
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.146T>C
  hgvsp: ENSP00000373392.3:p.Phe49Ser
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.245T>C
  hgvsp: ENSP00000303221.7:p.Phe82Ser
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2629
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe82Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

8-72234472-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234472
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234472
    reference: chr 8
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.234A>G
  hgvsp: ENST00000388743.2:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.410A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.234A>G
  hgvsp: ENST00000340726.3:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.135A>G
  hgvsp: ENST00000388740.3:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.225A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.135A>G
  hgvsp: ENST00000388741.2:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.234A>G
  hgvsp: ENST00000465115.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.234A>G
  hgvsp: ENST00000419131.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.234A>G
  hgvsp: ENST00000388742.4:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.234A>G
  hgvsp: ENST00000303824.7:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7159
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro78Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-72234476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234476
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234476
    reference: chr 8
allele count: 2
allele frequency: 1.657302905251993e-5
allele num: 120678
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.230G>A
  hgvsp: ENSP00000342626.3:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.230G>A
  hgvsp: ENSP00000303221.7:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.131G>A
  hgvsp: ENSP00000373393.2:p.Arg44Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.131G>A
  hgvsp: ENSP00000373392.3:p.Arg44Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.230G>A
  hgvsp: ENSP00000373394.4:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.230G>A
  hgvsp: ENSP00000373395.2:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.406G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.230G>A
  hgvsp: ENSP00000428391.1:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.230G>A
  hgvsp: ENSP00000410176.1:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.221G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg77Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

8-72234500-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234500
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234500
    reference: chr 8
allele count: 1
allele frequency: 8.30592378484335e-6
allele num: 120396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.206T>C
  hgvsp: ENSP00000410176.1:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.107T>C
  hgvsp: ENSP00000373393.2:p.Ile36Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.197T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.382T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.107T>C
  hgvsp: ENSP00000373392.3:p.Ile36Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.206T>C
  hgvsp: ENSP00000373395.2:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.206T>C
  hgvsp: ENSP00000428391.1:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.206T>C
  hgvsp: ENSP00000342626.3:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.206T>C
  hgvsp: ENSP00000373394.4:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.206T>C
  hgvsp: ENSP00000303221.7:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3500
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile69Thr
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

8-72234512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234512
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234512
    reference: chr 8
allele count: 1
allele frequency: 8.324176738920521e-6
allele num: 120132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.185G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.203-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.203-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.203-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.203-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.203-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.203-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.379-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.104-9G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.104-9G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-72234518-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234518
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234519
    reference: chr 8
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.178dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.203-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.104-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.203-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.203-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.203-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.379-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.203-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.203-16dupT
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.104-16dupT
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18863
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

8-72234518-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234518
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234518
    reference: chr 8
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.104-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.203-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.203-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.203-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.203-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.379-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.203-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.203-15G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.179G>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.104-15G>C
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-72234528-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234528
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234528
    reference: chr 8
allele count: 1
allele frequency: 8.367780697203488e-6
allele num: 119506
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.169A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.203-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.104-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.203-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.379-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.203-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.104-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.203-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.203-25A>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.203-25A>C
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24402
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

8-72234529-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234529
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234529
    reference: chr 8
allele count: 1
allele frequency: 8.355335717389125e-6
allele num: 119684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.203-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.203-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.203-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.203-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.203-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.203-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.104-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.104-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.379-26T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.168T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15107
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13475
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-72234540-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234540
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234540
    reference: chr 8
allele count: 1
allele frequency: 8.382229673093043e-6
allele num: 119300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.203-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.157T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.203-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.203-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.203-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.203-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.203-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.104-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.104-37T>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.379-37T>A
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 4.75e1
  variant carriers: 0
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: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

8-72234547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72234547
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72234547
    reference: chr 8
allele count: 161
allele frequency: 1.357916399581661e-3
allele num: 118564
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.203-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.203-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.379-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.203-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.203-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.203-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000422295
  gene symbol: EYA1
  hgvsc: ENST00000422295.1:n.150G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.104-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.104-44G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.203-44G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14509
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2984
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2250
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-72246283-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246283
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246283
    reference: chr 8
allele count: 1
allele frequency: 8.31766839119658e-6
allele num: 120226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202+49A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378+49A>G
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2920
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

8-72246306-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246306
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246306
    reference: chr 8
allele count: 204
allele frequency: 1.691598394639955e-3
allele num: 120596
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103+26C>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378+26C>A
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 14748
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12458
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7144
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-72246313-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246313
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246313
    reference: chr 8
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103+19A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103+19A>T
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21071
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2917
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-72246314-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246314
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246313
    reference: chr 8
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378+17delA
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202+17delA
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16724
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7218
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: CT
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

8-72246323-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246323
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246323
    reference: chr 8
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202+9T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202+9T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

8-72246324-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246324
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246324
    reference: chr 8
allele count: 3
allele frequency: 2.480897092388608e-5
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202+8A>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202+8A>T
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: c.202+8A>T
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

8-72246331-C-CGTAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246331
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246335
    reference: chr 8
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: CGTAA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202_202+1insTTAC
  hgvsp: ENSP00000373394.4:p.Ala68ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202_202+1insTTAC
  hgvsp: ENSP00000410176.1:p.Ala68ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202_202+1insTTAC
  hgvsp: ENSP00000342626.3:p.Ala68ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103_103+1insTTAC
  hgvsp: ENSP00000373393.2:p.Ala35ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202_202+1insTTAC
  hgvsp: ENSP00000428391.1:p.Ala68ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103_103+1insTTAC
  hgvsp: ENSP00000373392.3:p.Ala35ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202_202+1insTTAC
  hgvsp: ENSP00000303221.7:p.Ala68ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378_378+1insTTAC
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202_202+1insTTAC
  hgvsp: ENSP00000373395.2:p.Ala68ValfsTer7
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala68ValfsTer7
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

8-72246331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246331
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246331
    reference: chr 8
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.103+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.378+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.202+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.202+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.103+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.202+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.202+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.202+1G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.202+1G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
hgvs: c.202+1G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-72246337-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246337
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246337
    reference: chr 8
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.197G>T
  hgvsp: ENSP00000303221.7:p.Gly66Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.98G>T
  hgvsp: ENSP00000373393.2:p.Gly33Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.197G>T
  hgvsp: ENSP00000428391.1:p.Gly66Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.197G>T
  hgvsp: ENSP00000373395.2:p.Gly66Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.373G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.197G>T
  hgvsp: ENSP00000342626.3:p.Gly66Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.98G>T
  hgvsp: ENSP00000373392.3:p.Gly33Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.197G>T
  hgvsp: ENSP00000373394.4:p.Gly66Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.197G>T
  hgvsp: ENSP00000410176.1:p.Gly66Val
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4323
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16722
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly66Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

8-72246359-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246359
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246359
    reference: chr 8
allele count: 3
allele frequency: 2.477127852825577e-5
allele num: 121108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.175G>A
  hgvsp: ENSP00000373395.2:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.76G>A
  hgvsp: ENSP00000373393.2:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.76G>A
  hgvsp: ENSP00000373392.3:p.Gly26Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.175G>A
  hgvsp: ENSP00000373394.4:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.175G>A
  hgvsp: ENSP00000303221.7:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.175G>A
  hgvsp: ENSP00000410176.1:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.175G>A
  hgvsp: ENSP00000428391.1:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.175G>A
  hgvsp: ENSP00000342626.3:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.351G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly59Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

8-72246360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246360
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246360
    reference: chr 8
allele count: 8
allele frequency: 6.604910751143475e-5
allele num: 121122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.75C>T
  hgvsp: ENST00000388741.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.174C>T
  hgvsp: ENST00000388742.4:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.174C>T
  hgvsp: ENST00000388743.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.174C>T
  hgvsp: ENST00000340726.3:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.174C>T
  hgvsp: ENST00000419131.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.174C>T
  hgvsp: ENST00000465115.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.174C>T
  hgvsp: ENST00000303824.7:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.350C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.75C>T
  hgvsp: ENST00000388740.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp58Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

8-72246362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246362
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246362
    reference: chr 8
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.348G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.172G>A
  hgvsp: ENSP00000373395.2:p.Asp58Asn
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.172G>A
  hgvsp: ENSP00000428391.1:p.Asp58Asn
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.73G>A
  hgvsp: ENSP00000373392.3:p.Asp25Asn
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.172G>A
  hgvsp: ENSP00000303221.7:p.Asp58Asn
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.172G>A
  hgvsp: ENSP00000410176.1:p.Asp58Asn
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.172G>A
  hgvsp: ENSP00000373394.4:p.Asp58Asn
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.172G>A
  hgvsp: ENSP00000342626.3:p.Asp58Asn
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.73G>A
  hgvsp: ENSP00000373393.2:p.Asp25Asn
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp58Asn
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

8-72246363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246363
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246363
    reference: chr 8
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.171C>T
  hgvsp: ENST00000340726.3:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.171C>T
  hgvsp: ENST00000303824.7:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.171C>T
  hgvsp: ENST00000465115.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.72C>T
  hgvsp: ENST00000388740.3:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.171C>T
  hgvsp: ENST00000388742.4:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.72C>T
  hgvsp: ENST00000388741.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.171C>T
  hgvsp: ENST00000419131.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.347C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.171C>T
  hgvsp: ENST00000388743.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21679
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala57Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-72246369-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246369
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246369
    reference: chr 8
allele count: 2
allele frequency: 1.651091371396493e-5
allele num: 121132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.165G>T
  hgvsp: ENST00000465115.1:c.165G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.165G>T
  hgvsp: ENST00000388743.2:c.165G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.341G>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.165G>T
  hgvsp: ENST00000419131.1:c.165G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.165G>T
  hgvsp: ENST00000303824.7:c.165G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.165G>T
  hgvsp: ENST00000388742.4:c.165G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.165G>T
  hgvsp: ENST00000340726.3:c.165G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.66G>T
  hgvsp: ENST00000388741.2:c.66G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.66G>T
  hgvsp: ENST00000388740.3:c.66G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr55Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

8-72246369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246369
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246369
    reference: chr 8
allele count: 5
allele frequency: 4.127728428491233e-5
allele num: 121132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.165G>A
  hgvsp: ENST00000465115.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.66G>A
  hgvsp: ENST00000388741.2:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.165G>A
  hgvsp: ENST00000340726.3:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.165G>A
  hgvsp: ENST00000388743.2:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.165G>A
  hgvsp: ENST00000388742.4:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.165G>A
  hgvsp: ENST00000303824.7:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.165G>A
  hgvsp: ENST00000419131.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.341G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.66G>A
  hgvsp: ENST00000388740.3:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16724
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr55Thr
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-72246370-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246370
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246370
    reference: chr 8
allele count: 21
allele frequency: 1.733617316360394e-4
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.164C>T
  hgvsp: ENSP00000303221.7:p.Thr55Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.164C>T
  hgvsp: ENSP00000410176.1:p.Thr55Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.65C>T
  hgvsp: ENSP00000373392.3:p.Thr22Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.164C>T
  hgvsp: ENSP00000373395.2:p.Thr55Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.164C>T
  hgvsp: ENSP00000428391.1:p.Thr55Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.164C>T
  hgvsp: ENSP00000373394.4:p.Thr55Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.65C>T
  hgvsp: ENSP00000373393.2:p.Thr22Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.164C>T
  hgvsp: ENSP00000342626.3:p.Thr55Met
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.340C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr55Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

8-72246371-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246371
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246371
    reference: chr 8
allele count: 3
allele frequency: 2.476677949310658e-5
allele num: 121130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.339A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.163A>G
  hgvsp: ENSP00000428391.1:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.163A>G
  hgvsp: ENSP00000373395.2:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.163A>G
  hgvsp: ENSP00000303221.7:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.64A>G
  hgvsp: ENSP00000373393.2:p.Thr22Ala
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.163A>G
  hgvsp: ENSP00000373394.4:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.163A>G
  hgvsp: ENSP00000410176.1:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.163A>G
  hgvsp: ENSP00000342626.3:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.64A>G
  hgvsp: ENSP00000373392.3:p.Thr22Ala
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr55Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

8-72246375-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246375
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246375
    reference: chr 8
allele count: 3
allele frequency: 2.476596166229135e-5
allele num: 121134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.335T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.159T>C
  hgvsp: ENST00000419131.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.159T>C
  hgvsp: ENST00000303824.7:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.159T>C
  hgvsp: ENST00000465115.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.60T>C
  hgvsp: ENST00000388740.3:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.159T>C
  hgvsp: ENST00000388743.2:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.159T>C
  hgvsp: ENST00000388742.4:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.60T>C
  hgvsp: ENST00000388741.2:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.159T>C
  hgvsp: ENST00000340726.3:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7270
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala53Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

8-72246376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246376
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246376
    reference: chr 8
allele count: 1
allele frequency: 8.255184255712587e-6
allele num: 121136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.158C>T
  hgvsp: ENSP00000373395.2:p.Ala53Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.158C>T
  hgvsp: ENSP00000342626.3:p.Ala53Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.59C>T
  hgvsp: ENSP00000373392.3:p.Ala20Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.59C>T
  hgvsp: ENSP00000373393.2:p.Ala20Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.158C>T
  hgvsp: ENSP00000373394.4:p.Ala53Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.158C>T
  hgvsp: ENSP00000303221.7:p.Ala53Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.158C>T
  hgvsp: ENSP00000410176.1:p.Ala53Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.158C>T
  hgvsp: ENSP00000428391.1:p.Ala53Val
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.334C>T
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala53Val
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ

8-72246379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246379
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246379
    reference: chr 8
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.331C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.155C>T
  hgvsp: ENSP00000303221.7:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.155C>T
  hgvsp: ENSP00000428391.1:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.155C>T
  hgvsp: ENSP00000410176.1:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.56C>T
  hgvsp: ENSP00000373392.3:p.Thr19Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.155C>T
  hgvsp: ENSP00000342626.3:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.155C>T
  hgvsp: ENSP00000373395.2:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.56C>T
  hgvsp: ENSP00000373393.2:p.Thr19Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.155C>T
  hgvsp: ENSP00000373394.4:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr52Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

8-72246387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246387
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246387
    reference: chr 8
allele count: 20
allele frequency: 1.651200422707308e-4
allele num: 121124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.48C>T
  hgvsp: ENST00000388740.3:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.147C>T
  hgvsp: ENST00000388743.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.323C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.147C>T
  hgvsp: ENST00000388742.4:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.147C>T
  hgvsp: ENST00000303824.7:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.147C>T
  hgvsp: ENST00000465115.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.48C>T
  hgvsp: ENST00000388741.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.147C>T
  hgvsp: ENST00000419131.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.147C>T
  hgvsp: ENST00000340726.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10363
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser49Ser
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

8-72246403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246403
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246403
    reference: chr 8
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.131C>T
  hgvsp: ENSP00000342626.3:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.131C>T
  hgvsp: ENSP00000303221.7:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.131C>T
  hgvsp: ENSP00000373394.4:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.32C>T
  hgvsp: ENSP00000373393.2:p.Thr11Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.32C>T
  hgvsp: ENSP00000373392.3:p.Thr11Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.131C>T
  hgvsp: ENSP00000428391.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.307C>T
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.131C>T
  hgvsp: ENSP00000410176.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.131C>T
  hgvsp: ENSP00000373395.2:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7256
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr44Ile
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

8-72246411-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246411
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246411
    reference: chr 8
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.125-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.26-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.26-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.301-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.125-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.125-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.125-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.125-2A>G
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.125-2A>G
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12552
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7256
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21352
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4310
  bin: 7.75e1
  variant carriers: 0
hgvs: c.125-2A>G
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

8-72246420-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246420
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246420
    reference: chr 8
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.125-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.26-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.125-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.125-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.125-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.26-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.125-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.301-11T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.125-11T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10366
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16717
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7230
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

8-72246422-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246422
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246422
    reference: chr 8
allele count: 1
allele frequency: 8.270477702792114e-6
allele num: 120912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.125-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.125-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.26-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.125-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.125-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.125-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.125-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.301-13T>C
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.26-13T>C
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

8-72246423-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72246423
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 72246423
    reference: chr 8
allele count: 2
allele frequency: 1.654533421575116e-5
allele num: 120880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373392
  ensembl transcript: ENST00000388740
  gene symbol: EYA1
  hgvsc: ENST00000388740.3:c.26-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000410176
  ensembl transcript: ENST00000419131
  gene symbol: EYA1
  hgvsc: ENST00000419131.1:c.125-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000428391
  ensembl transcript: ENST00000465115
  gene symbol: EYA1
  hgvsc: ENST00000465115.1:c.125-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000303221
  ensembl transcript: ENST00000303824
  gene symbol: EYA1
  hgvsc: ENST00000303824.7:c.125-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373394
  ensembl transcript: ENST00000388742
  gene symbol: EYA1
  hgvsc: ENST00000388742.4:c.125-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl transcript: ENST00000496494
  gene symbol: EYA1
  hgvsc: ENST00000496494.1:n.301-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373395
  ensembl transcript: ENST00000388743
  gene symbol: EYA1
  hgvsc: ENST00000388743.2:c.125-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000342626
  ensembl transcript: ENST00000340726
  gene symbol: EYA1
  hgvsc: ENST00000340726.3:c.125-14G>A
  variant of: http://identifiers.org/hgnc/3519
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104313
  ensembl protein: ENSP00000373393
  ensembl transcript: ENST00000388741
  gene symbol: EYA1
  hgvsc: ENST00000388741.2:c.26-14G>A
  variant of: http://identifiers.org/hgnc/3519
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16717
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3528
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C

GenotypeQuality
all individuals: 1694
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3113
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5746
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1455
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

FS
type: SiteQuality
SIO_000300: 5.002e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.266e0

QD
type: SiteQuality
SIO_000300: 1.307e1

DP
type: SiteQuality
SIO_000300: 1.624639e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5742
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 5.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

DP
type: SiteQuality
SIO_000300: 1.624791e6

QD
type: SiteQuality
SIO_000300: 1.216e1

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

GenotypeQuality
all individuals: 490
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5745
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
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: 1151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 7.75e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 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: 11572
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: 66730
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.555e0

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

FS
type: SiteQuality
SIO_000300: 5.161e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

DP
type: SiteQuality
SIO_000300: 1.624837e6

QD
type: SiteQuality
SIO_000300: 1.149e1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e-1

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

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

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

GenotypeQuality
all individuals: 5745
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 46417
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.61e-1

DP
type: SiteQuality
SIO_000300: 1.624837e6

QD
type: SiteQuality
SIO_000300: 1.149e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

FS
type: SiteQuality
SIO_000300: 5.161e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.555e0

GenotypeQuality
all individuals: 1691
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1454
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 9.75e1
variant carriers: 4

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: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.995e0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 1.624156e6

QD
type: SiteQuality
SIO_000300: 1.077e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

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

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

GenotypeQuality
all individuals: 1689
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3108
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
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: 8636
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: 16510
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.065e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 1.383e1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQ
type: SiteQuality
SIO_000300: 5.847e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.623569e6

VQSLOD
type: SiteQuality
SIO_000300: -2.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

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

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5724
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3108
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 46367
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1455
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 8.25e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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South Asian
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 4.499775011249437e-5
allele num: 66670
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

South Asian
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allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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DP
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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DP
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SIO_000300: 1.622412e6

MQ
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SIO_000300: 5.969e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

South Asian
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BaseQRankSum
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SIO_000300: -1.376e0

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

ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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VQSLOD
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DP
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QD
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SIO_000300: 1.336e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

Other
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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allele frequency: 1.731002250302925e-4
allele num: 11554
num of homozygotes: 0

South Asian
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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Other
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South Asian
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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Other
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VQSLOD
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DP
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BaseQRankSum
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.737098344693281e-5
allele num: 10270
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.385e0

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

QD
type: SiteQuality
SIO_000300: 1.577e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.045e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

DP
type: SiteQuality
SIO_000300: 1.598725e6

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

GenotypeQuality
all individuals: 332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 7.75e1
variant carriers: 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: 65748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.826817683595177e-4
allele num: 16422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.02e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.241e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.275e0

DP
type: SiteQuality
SIO_000300: 1.59008e6

GenotypeQuality
all individuals: 484
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
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variant carriers: 0

GenotypeQuality
all individuals: 41959
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.121021336131515e-4
allele num: 11436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529519730804527e-5
allele num: 65380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

DP
type: SiteQuality
SIO_000300: 1.571761e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.405e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

GenotypeQuality
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42106
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
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variant carriers: 0

GenotypeQuality
all individuals: 1380
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variant carriers: 0

GenotypeQuality
all individuals: 531
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variant carriers: 0

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

GenotypeQuality
all individuals: 1635
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variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
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variant carriers: 0

GenotypeQuality
all individuals: 5324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529706908156397e-5
allele num: 65372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.804e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
SIO_000300: -8.051e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.93e0

FS
type: SiteQuality
SIO_000300: 2.0264e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

DP
type: SiteQuality
SIO_000300: 1.571503e6

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6003
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variant carriers: 0

GenotypeQuality
all individuals: 483
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variant carriers: 0

GenotypeQuality
all individuals: 1870
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variant carriers: 0

GenotypeQuality
all individuals: 210
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GenotypeQuality
all individuals: 4975
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variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
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variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 579
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variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35991
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.915e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.795e0

QD
type: SiteQuality
SIO_000300: 5.13e0

DP
type: SiteQuality
SIO_000300: 1.502352e6

MQ
type: SiteQuality
SIO_000300: 5.748e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.413e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.899e0

GenotypeQuality
all individuals: 110
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2731
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3735
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3101
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3496
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
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variant carriers: 0

GenotypeQuality
all individuals: 1090
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variant carriers: 0

GenotypeQuality
all individuals: 7442
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15053
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variant carriers: 0

GenotypeQuality
all individuals: 701
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variant carriers: 0

GenotypeQuality
all individuals: 1477
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 578
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variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.621796951021732e-5
allele num: 61660
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

QD
type: SiteQuality
SIO_000300: 1.307e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

DP
type: SiteQuality
SIO_000300: 1.33054e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

GenotypeQuality
all individuals: 925
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 479
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variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1471
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variant carriers: 0

GenotypeQuality
all individuals: 1861
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variant carriers: 0

GenotypeQuality
all individuals: 899
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variant carriers: 0

GenotypeQuality
all individuals: 3102
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2911
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1088
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variant carriers: 0

GenotypeQuality
all individuals: 3069
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
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GenotypeQuality
all individuals: 1086
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variant carriers: 0

GenotypeQuality
all individuals: 6582
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.370614035087719e-4
allele num: 7296
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.046e1

VQSLOD
type: SiteQuality
SIO_000300: -5.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.098e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 1.322687e6

GenotypeQuality
all individuals: 1064
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

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

GenotypeQuality
all individuals: 6344
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variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.813678829543451e-5
allele num: 11346
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65556
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.425e1

MQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

DP
type: SiteQuality
SIO_000300: 2.086882e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
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GenotypeQuality
all individuals: 419
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13472
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variant carriers: 1

GenotypeQuality
all individuals: 1349
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
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GenotypeQuality
all individuals: 3416
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variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2259
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17206
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.807468733485996e-5
allele num: 11354
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65518
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10150
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

QD
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SIO_000300: 1.172e1

MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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SIO_000300: -1.732e0

FS
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.977e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.024254521260509e-5
allele num: 66132
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

DP
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SIO_000300: 2.175271e6

ClippingRankSum
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SIO_000300: 3.52e-1

QD
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BaseQRankSum
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SIO_000300: -1.903e0

MQRankSum
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SIO_000300: 1.76e0

VQSLOD
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SIO_000300: -3.861e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

ReadPosRankSum
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SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 1.209e0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

QD
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VQSLOD
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SIO_000300: 6.2e-1

FS
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
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SIO_000300: 7.51e-1

DP
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SIO_000300: 2.184497e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 3
allele frequency: 2.918855808523059e-4
allele num: 10278
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

FS
type: SiteQuality
SIO_000300: 1.953e0

MQRankSum
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SIO_000300: -9.84e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
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SIO_000300: 1.86e0

ClippingRankSum
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SIO_000300: -3.66e-1

DP
type: SiteQuality
SIO_000300: 2.185318e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.176e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.831e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014045451805413e-5
allele num: 66356
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -1.081e0

MQ
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SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 3.938e0

ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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SIO_000300: 1.68e-1

ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

Latino
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allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 3.96e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Other
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66366
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6606
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Latino
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African
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South Asian
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allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
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Other
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele num: 10272
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DP
type: SiteQuality
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11502
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European (Non-Finnish)
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allele frequency: 1.507022725902707e-5
allele num: 66356
num of homozygotes: 0

MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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SIO_000300: 8.96e-1

ClippingRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
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SIO_000300: 0.0e0

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

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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East Asian
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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FS
type: SiteQuality
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QD
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MQ
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.015317814497648e-5
allele num: 66328
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

African
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East Asian
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Other
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num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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ClippingRankSum
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DP
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MQ
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10212
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Other
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European (Finnish)
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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African
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QD
type: SiteQuality
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VQSLOD
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DP
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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allele num: 66040
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African
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Latino
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allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.108e1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

FS
type: SiteQuality
SIO_000300: 1.234e0

DP
type: SiteQuality
SIO_000300: 2.175597e6

MQ
type: SiteQuality
SIO_000300: 5.905e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.898e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514233797698365e-5
allele num: 66040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

FS
type: SiteQuality
SIO_000300: 1.234e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.898e0

QD
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SIO_000300: 1.108e1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.22e-1

DP
type: SiteQuality
SIO_000300: 2.175597e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520172691617768e-5
allele num: 65782
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

MQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.597e0

QD
type: SiteQuality
SIO_000300: 5.99e0

FS
type: SiteQuality
SIO_000300: 2.573e0

DP
type: SiteQuality
SIO_000300: 2.159895e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.8e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 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: 16334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518233990222573e-5
allele num: 65866
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.221e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 2.158408e6

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

FS
type: SiteQuality
SIO_000300: 2.741e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 1.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 13464
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.972078181092939e-5
allele num: 10028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65668
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

FS
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 8.91e0

MQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

DP
type: SiteQuality
SIO_000300: 2.12621e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 159

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

GenotypeQuality
all individuals: 5411
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variant carriers: 0

Latino
type: Population
allele count: 10
allele frequency: 8.882572392965003e-4
allele num: 11258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.143553794574825e-4
allele num: 6562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.02108857200241e-4
allele num: 9958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 113
allele frequency: 1.730580740014702e-3
allele num: 65296
num of homozygotes: 0

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

South Asian
type: Population
allele count: 27
allele frequency: 1.665844027640671e-3
allele num: 16208
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

DP
type: SiteQuality
SIO_000300: 2.104288e6

QD
type: SiteQuality
SIO_000300: 1.321e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
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SIO_000300: 1.1e0

ClippingRankSum
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SIO_000300: -2.922e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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QD
type: SiteQuality
SIO_000300: 2.007e1

DP
type: SiteQuality
SIO_000300: 2.25491e6

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.532332209623046e-4
allele num: 6526
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 2
allele frequency: 1.751006828926633e-4
allele num: 11422
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African
type: Population
allele count: 8
allele frequency: 7.716049382716049e-4
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 193
allele frequency: 2.910308221243742e-3
allele num: 66316
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 7.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e0

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

DP
type: SiteQuality
SIO_000300: 2.301969e6

MQ
type: SiteQuality
SIO_000300: 5.987e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 86
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
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: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
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DP
type: SiteQuality
SIO_000300: 2.302935e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.118e0

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

FS
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MQRankSum
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ReadPosRankSum
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SIO_000300: 2.09e0

VQSLOD
type: SiteQuality
SIO_000300: -6.608000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 1.29e-1

FS
type: SiteQuality
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.303527e6

BaseQRankSum
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SIO_000300: -2.457e0

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

Other
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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: 10374
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.732099196646873e-5
allele num: 11452
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

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

MQRankSum
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SIO_000300: 9.05e-1

VQSLOD
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SIO_000300: -4.831e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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DP
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SIO_000300: 2.306096e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.142e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

QD
type: SiteQuality
SIO_000300: 1.617e1

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

Latino
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allele count: 3
allele frequency: 2.618715083798883e-4
allele num: 11456
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66508
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.418e1

DP
type: SiteQuality
SIO_000300: 2.306392e6

MQRankSum
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SIO_000300: -1.82e-1

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 2.63e-1

BaseQRankSum
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SIO_000300: 2.17e0

VQSLOD
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SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

MQ
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SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

BaseQRankSum
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SIO_000300: 2.26e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

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

DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 1.05e0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

South Asian
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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MQ
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SIO_000300: 5.811e1

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

African
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num of homozygotes: 0

East Asian
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allele frequency: 2.314279102059708e-4
allele num: 8642
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
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FS
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.008738476322033e-5
allele num: 66602
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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South Asian
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African
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allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

East Asian
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

ClippingRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
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FS
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SIO_000300: 5.21e-1

QD
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DP
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MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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SIO_000300: 2.83e0

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

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

Latino
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allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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FS
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MQ
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SIO_000300: 5.936e1

DP
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QD
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MQRankSum
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BaseQRankSum
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SIO_000300: -6.5e-1

ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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DP
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QD
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
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Latino
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allele frequency: 0.0e0
allele num: 11492
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16506
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Other
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002552169343942e-5
allele num: 66610
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.310236e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
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allele count: 18
allele frequency: 2.702296952409548e-4
allele num: 66610
num of homozygotes: 0

South Asian
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allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQRankSum
type: SiteQuality
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FS
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 2.311412e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele num: 10398
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South Asian
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allele num: 16506
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European (Finnish)
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European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

Other
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Other
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.211680600993578e-4
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European (Non-Finnish)
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allele count: 1
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allele num: 66610
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66610
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European (Finnish)
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South Asian
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African
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21689
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.309625e6

MQRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.432e0

QD
type: SiteQuality
SIO_000300: 1.448e1

FS
type: SiteQuality
SIO_000300: 7.415e0

VQSLOD
type: SiteQuality
SIO_000300: -3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.52e-1

GenotypeQuality
all individuals: 4314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 21655
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2923
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7265
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 20
allele frequency: 2.314279102059709e-3
allele num: 8642
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.802e0

DP
type: SiteQuality
SIO_000300: 2.310528e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 5.35e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.12e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

GenotypeQuality
all individuals: 2408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1634
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4311
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16717
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2922
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21496
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 2.586e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.973e0

DP
type: SiteQuality
SIO_000300: 2.30793e6

MQRankSum
type: SiteQuality
SIO_000300: -1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

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

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

GenotypeQuality
all individuals: 2921
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 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: 6566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 2.427e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -2.635e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 2.806e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

DP
type: SiteQuality
SIO_000300: 2.306709e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21088
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2914
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
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: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e0

FS
type: SiteQuality
SIO_000300: 1.306e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

DP
type: SiteQuality
SIO_000300: 2.304433e6

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

QD
type: SiteQuality
SIO_000300: 1.495e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

GenotypeQuality
all individuals: 2915
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20984
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16715
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 4308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 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: 1.503804625703029e-5
allele num: 66498
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 3.721e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

QD
type: SiteQuality
SIO_000300: 1.469e1

MQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

DP
type: SiteQuality
SIO_000300: 2.303394e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 20687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
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: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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