8-24190222-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190222
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190222
    reference: chr 8
allele count: 4
allele frequency: 3.315045333244932e-5
allele num: 120662
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.632C>G
  hgvsp: ENSP00000443743.1:p.Thr211Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.228C>G
  hgvsp: ENSP00000429484.1:p.Thr77Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31780G>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1331C>G
  hgvsp: ENSP00000265769.4:p.Thr444Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31780G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.572C>G
  hgvsp: ENSP00000380770.3:p.Thr191Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31780G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042980
  ensembl transcript: ENST00000521110
  gene symbol: ADAM28
  hgvsc: ENST00000521110.1:n.494C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*739C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1331C>G
  hgvsp: ENSP00000393699.2:p.Thr444Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31780G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr444Ser
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-24190222-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190222
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190222
    reference: chr 8
allele count: 2
allele frequency: 1.657522666622466e-5
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31780G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1331C>T
  hgvsp: ENSP00000265769.4:p.Thr444Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1331C>T
  hgvsp: ENSP00000393699.2:p.Thr444Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042980
  ensembl transcript: ENST00000521110
  gene symbol: ADAM28
  hgvsc: ENST00000521110.1:n.494C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31780G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31780G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.632C>T
  hgvsp: ENSP00000443743.1:p.Thr211Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*739C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.572C>T
  hgvsp: ENSP00000380770.3:p.Thr191Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.228C>T
  hgvsp: ENSP00000429484.1:p.Thr77Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31780G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr444Ile
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

8-24190225-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190225
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190225
    reference: chr 8
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31783A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042980
  ensembl transcript: ENST00000521110
  gene symbol: ADAM28
  hgvsc: ENST00000521110.1:n.497T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31783A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31783A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.635T>G
  hgvsp: ENSP00000443743.1:p.Phe212Cys
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1334T>G
  hgvsp: ENSP00000393699.2:p.Phe445Cys
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.231T>G
  hgvsp: ENSP00000429484.1:p.Phe78Cys
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1334T>G
  hgvsp: ENSP00000265769.4:p.Phe445Cys
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*742T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.575T>G
  hgvsp: ENSP00000380770.3:p.Phe192Cys
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31783A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe445Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

8-24190226-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190226
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190226
    reference: chr 8
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.232T>C
  hgvsp: ENST00000521629.1:c.232T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*743T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042980
  ensembl transcript: ENST00000521110
  gene symbol: ADAM28
  hgvsc: ENST00000521110.1:n.498T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1335T>C
  hgvsp: ENST00000437154.2:c.1335T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31784A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31784A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31784A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1335T>C
  hgvsp: ENST00000265769.4:c.1335T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.636T>C
  hgvsp: ENST00000540823.1:c.636T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31784A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.576T>C
  hgvsp: ENST00000397649.3:c.576T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe445Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

8-24190231-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190231
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190231
    reference: chr 8
allele count: 9
allele frequency: 7.467392386578607e-5
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*748G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.641G>A
  hgvsp: ENSP00000443743.1:p.Cys214Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1340G>A
  hgvsp: ENSP00000265769.4:p.Cys447Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.237G>A
  hgvsp: ENSP00000429484.1:p.Cys80Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31789C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31789C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.581G>A
  hgvsp: ENSP00000380770.3:p.Cys194Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31789C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1340G>A
  hgvsp: ENSP00000393699.2:p.Cys447Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042980
  ensembl transcript: ENST00000521110
  gene symbol: ADAM28
  hgvsc: ENST00000521110.1:n.503G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31789C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10422
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys447Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-24190233-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190233
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190233
    reference: chr 8
allele count: 1
allele frequency: 8.300132802124834e-6
allele num: 120480
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1342G>A
  hgvsp: ENSP00000265769.4:p.Ala448Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31791C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042980
  ensembl transcript: ENST00000521110
  gene symbol: ADAM28
  hgvsc: ENST00000521110.1:n.505G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31791C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.583G>A
  hgvsp: ENSP00000380770.3:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31791C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*750G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.643G>A
  hgvsp: ENSP00000443743.1:p.Ala215Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1342G>A
  hgvsp: ENSP00000393699.2:p.Ala448Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.239G>A
  hgvsp: ENSP00000429484.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31791C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala448Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

8-24190249-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190249
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190249
    reference: chr 8
allele count: 5
allele frequency: 4.185851820845542e-5
allele num: 119450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.599G>T
  hgvsp: ENSP00000380770.3:p.Cys200Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31807C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.659G>T
  hgvsp: ENSP00000443743.1:p.Cys220Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1358G>T
  hgvsp: ENSP00000265769.4:p.Cys453Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.255G>T
  hgvsp: ENSP00000429484.1:p.Cys86Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31807C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31807C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1358G>T
  hgvsp: ENSP00000393699.2:p.Cys453Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31807C>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*766G>T
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20474
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys453Phe
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

8-24190257-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190257
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190257
    reference: chr 8
allele count: 1
allele frequency: 8.553880895762407e-6
allele num: 116906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.607T>C
  hgvsp: ENSP00000380770.3:p.Cys203Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1366T>C
  hgvsp: ENSP00000393699.2:p.Cys456Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31815A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.263T>C
  hgvsp: ENSP00000429484.1:p.Cys89Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31815A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*774T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31815A>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1366T>C
  hgvsp: ENSP00000265769.4:p.Cys456Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.667T>C
  hgvsp: ENSP00000443743.1:p.Cys223Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31815A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16075
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7486
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys456Arg
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-24190258-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190258
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190258
    reference: chr 8
allele count: 3
allele frequency: 2.578515806301893e-5
allele num: 116346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1367G>T
  hgvsp: ENSP00000393699.2:p.Cys456Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31816C>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1367G>T
  hgvsp: ENSP00000265769.4:p.Cys456Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.668G>T
  hgvsp: ENSP00000443743.1:p.Cys223Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31816C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31816C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.264G>T
  hgvsp: ENSP00000429484.1:p.Cys89Phe
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*775G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31816C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.608G>T
  hgvsp: ENSP00000380770.3:p.Cys203Phe
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys456Phe
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-24190262-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190262
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190262
    reference: chr 8
allele count: 5
allele frequency: 4.388351559620144e-5
allele num: 113938
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31820T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371A>G
  hgvsp: ENST00000437154.2:c.1371A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31820T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672A>G
  hgvsp: ENST00000540823.1:c.672A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371A>G
  hgvsp: ENST00000265769.4:c.1371A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268A>G
  hgvsp: ENST00000521629.1:c.268A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612A>G
  hgvsp: ENST00000397649.3:c.612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31820T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31820T>C
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14857
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13043
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2951
  bin: 9.75e1
  variant carriers: 5
hgvs: c.1371A>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-24190266-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190266
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190266
    reference: chr 8
allele count: 1
allele frequency: 9.152982957145734e-6
allele num: 109254
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+4A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+4A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31824T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31824T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31824T>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+4A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+4A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+4A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+4A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31824T>G
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16722
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1371+4A>C
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

8-24190268-A-ATTAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190268
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190272
    reference: chr 8
allele count: 1
allele frequency: 9.346667912889055e-6
allele num: 106990
alternate allele: ATTAT
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31830_356-31827dupATAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31830_502-31827dupATAA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+9_268+12dupATTT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+9_1371+12dupATTT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+9_1371+12dupATTT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+9_672+12dupATTT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31830_607-31827dupATAA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+9_*779+12dupATTT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+9_612+12dupATTT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31830_165-31827dupATAA
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1371+9_1371+12dupATTT
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

8-24190284-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190284
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190284
    reference: chr 8
allele count: 1
allele frequency: 1.350438892640108e-5
allele num: 74050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31842A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31842A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+22T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+22T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+22T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31842A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+22T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+22T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31842A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+22T>C
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10039
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-24190292-TATG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190292
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190289
    reference: chr 8
allele count: 280
allele frequency: 4.378557578032151e-3
allele num: 63948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+33_612+35delGAT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+33_672+35delGAT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+33_268+35delGAT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31853_502-31851delCAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31853_165-31851delCAT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+33_*779+35delGAT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31853_607-31851delCAT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+33_1371+35delGAT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+33_1371+35delGAT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31853_356-31851delCAT
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11511
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14302
  bin: 7.5e0
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 19718
  bin: 1.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 1.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11878
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21004
  bin: 2.25e1
  variant carriers: 2
num of homozygotes: 3
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: TATG
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

8-24190297-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190297
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190297
    reference: chr 8
allele count: 1
allele frequency: 1.691188905800778e-5
allele num: 59130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31855A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+35T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+35T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+35T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+35T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31855A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+35T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31855A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31855A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+35T>C
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15498
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4208
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3308
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-24190305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190305
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190305
    reference: chr 8
allele count: 1
allele frequency: 1.923668821175746e-5
allele num: 51984
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+43T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+43T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+43T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31863A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+43T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31863A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+43T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31863A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31863A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+43T>C
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14778
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18310
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13132
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4837
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum

8-24190305-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190305
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190305
    reference: chr 8
allele count: 1
allele frequency: 1.923668821175746e-5
allele num: 51984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+43T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+43T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+43T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31863A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31863A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+43T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+43T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31863A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+43T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31863A>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14778
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18310
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4837
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP

8-24190307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24190307
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24190307
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 49166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.672+45A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1371+45A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-31865T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-31865T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.612+45A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.268+45A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-31865T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-31865T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1371+45A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*779+45A>G
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19302
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3227
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4791
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4891
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-24192908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192908
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192908
    reference: chr 8
allele count: 1
allele frequency: 1.336826907651997e-5
allele num: 74804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34466C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-51G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34466C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-51G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-51G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-51G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34466C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34466C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-51G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-51G>A
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8848
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2668
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

8-24192910-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192910
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192910
    reference: chr 8
allele count: 6
allele frequency: 8.047857928481369e-5
allele num: 74554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-49T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34468A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-49T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-49T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-49T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-49T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-49T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34468A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34468A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34468A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19398
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 8360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

8-24192918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192918
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192918
    reference: chr 8
allele count: 51
allele frequency: 6.694846281078527e-4
allele num: 76178
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-41G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-41G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34476C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34476C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-41G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-41G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-41G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34476C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34476C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-41G>A
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19177
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18569
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16015
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 9.75e1
  variant carriers: 53
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

8-24192918-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192918
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192918
    reference: chr 8
allele count: 1
allele frequency: 1.312714957074221e-5
allele num: 76178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34476C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-41G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-41G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-41G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34476C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-41G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34476C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-41G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-41G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34476C>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19177
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5704
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/8-24192933-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192933
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192933
    reference: chr 8
allele count: 1
allele frequency: 1.203079884504331e-5
allele num: 83120
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-26A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34491T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34491T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34491T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-26A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34491T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-26A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-26A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-26A>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-26A>C
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

8-24192934-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192934
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192935
    reference: chr 8
allele count: 2
allele frequency: 2.385610000477122e-5
allele num: 83836
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34493dupG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-23dupC
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-23dupC
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-23dupC
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-23dupC
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34493dupG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-23dupC
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34493dupG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34493dupG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-23dupC
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21642
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16668
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum

8-24192936-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192936
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192936
    reference: chr 8
allele count: 1
allele frequency: 1.162034024356233e-5
allele num: 86056
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-23C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-23C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34494G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-23C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-23C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-23C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-23C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34494G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34494G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34494G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

8-24192941-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192941
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192942
    reference: chr 8
allele count: 7
allele frequency: 7.657302879145883e-5
allele num: 91416
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34500dupA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-13dupT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-13dupT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34500dupA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-13dupT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-13dupT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-13dupT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34500dupA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-13dupT
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34500dupA
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14089
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29319
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-24192941-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192941
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192941
    reference: chr 8
allele count: 16
allele frequency: 1.750240658090487e-4
allele num: 91416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-18A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-18A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34499T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-18A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34499T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34499T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-18A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-18A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-18A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34499T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29319
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2664
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31132
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

8-24192941-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192941
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192941
    reference: chr 8
allele count: 1
allele frequency: 1.093900411306555e-5
allele num: 91416
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31132
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2664
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3064
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13853
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.964096319283498e-5
  allele num: 50914
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5820
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9502
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6872
  num of homozygotes: 0
population: South Asian
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

8-24192948-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192948
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192948
    reference: chr 8
allele count: 1
allele frequency: 1.004782765965998e-5
allele num: 99524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34506A>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34506A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-11T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-11T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-11T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34506A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-11T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34506A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-11T>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-11T>G
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10407
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

8-24192954-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192954
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192954
    reference: chr 8
allele count: 1
allele frequency: 9.384384384384384e-6
allele num: 106560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-5T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-5T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34512A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34512A>G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-5T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-5T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34512A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-5T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34512A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-5T>C
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1372-5T>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-24192955-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192955
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192955
    reference: chr 8
allele count: 3
allele frequency: 2.792360102758852e-5
allele num: 107436
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1372-4A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.673-4A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34513T>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*780-4A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1372-4A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.269-4A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34513T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34513T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34513T>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.613-4A>G
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1372-4A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD

8-24192968-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192968
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192968
    reference: chr 8
allele count: 1
allele frequency: 8.669568082118148e-6
allele num: 115346
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34526C>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*789G>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34526C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1381G>C
  hgvsp: ENSP00000265769.4:p.Ala461Pro
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34526C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.278G>C
  hgvsp: ENSP00000429484.1:p.Ala94Pro
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1381G>C
  hgvsp: ENSP00000393699.2:p.Ala461Pro
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34526C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.682G>C
  hgvsp: ENSP00000443743.1:p.Ala228Pro
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.622G>C
  hgvsp: ENSP00000380770.3:p.Ala208Pro
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala461Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-24192971-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192971
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192971
    reference: chr 8
allele count: 1
allele frequency: 8.585164835164835e-6
allele num: 116480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.281G>A
  hgvsp: ENSP00000429484.1:p.Gly95Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34529C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.625G>A
  hgvsp: ENSP00000380770.3:p.Gly209Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1384G>A
  hgvsp: ENSP00000265769.4:p.Gly462Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34529C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*792G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34529C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.685G>A
  hgvsp: ENSP00000443743.1:p.Gly229Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34529C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1384G>A
  hgvsp: ENSP00000393699.2:p.Gly462Arg
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly462Arg
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

8-24192972-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192972
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192972
    reference: chr 8
allele count: 42
allele frequency: 3.598170073505474e-4
allele num: 116726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.626G>C
  hgvsp: ENSP00000380770.3:p.Gly209Ala
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34530C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.282G>C
  hgvsp: ENSP00000429484.1:p.Gly95Ala
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34530C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1385G>C
  hgvsp: ENSP00000265769.4:p.Gly462Ala
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34530C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1385G>C
  hgvsp: ENSP00000393699.2:p.Gly462Ala
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.686G>C
  hgvsp: ENSP00000443743.1:p.Gly229Ala
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34530C>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*793G>C
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 44878
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly462Ala
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

8-24192979-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192979
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192979
    reference: chr 8
allele count: 2
allele frequency: 1.694484453105143e-5
allele num: 118030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1392G>A
  hgvsp: ENST00000437154.2:c.1392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34537C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34537C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34537C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.693G>A
  hgvsp: ENST00000540823.1:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.633G>A
  hgvsp: ENST00000397649.3:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*800G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34537C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.289G>A
  hgvsp: ENST00000521629.1:c.289G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1392G>A
  hgvsp: ENST00000265769.4:c.1392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val464Val
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

8-24192983-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192983
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192983
    reference: chr 8
allele count: 2
allele frequency: 1.685857342751656e-5
allele num: 118634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.293A>G
  hgvsp: ENSP00000429484.1:p.Arg99Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34541T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.637A>G
  hgvsp: ENSP00000380770.3:p.Arg213Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*804A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.697A>G
  hgvsp: ENSP00000443743.1:p.Arg233Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34541T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1396A>G
  hgvsp: ENSP00000265769.4:p.Arg466Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1396A>G
  hgvsp: ENSP00000393699.2:p.Arg466Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34541T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34541T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg466Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

8-24192992-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24192992
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24192992
    reference: chr 8
allele count: 1
allele frequency: 8.353241893178742e-6
allele num: 119714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.706A>G
  hgvsp: ENSP00000443743.1:p.Lys236Glu
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34550T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.302A>G
  hgvsp: ENSP00000429484.1:p.Lys102Glu
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1405A>G
  hgvsp: ENSP00000265769.4:p.Lys469Glu
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.646A>G
  hgvsp: ENSP00000380770.3:p.Lys216Glu
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34550T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34550T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*813A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1405A>G
  hgvsp: ENSP00000393699.2:p.Lys469Glu
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34550T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys469Glu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

8-24193003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193003
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193003
    reference: chr 8
allele count: 2
allele frequency: 1.66220641279234e-5
allele num: 120322
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34561G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1416C>T
  hgvsp: ENST00000265769.4:c.1416C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34561G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34561G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.313C>T
  hgvsp: ENST00000521629.1:c.313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1416C>T
  hgvsp: ENST00000437154.2:c.1416C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.717C>T
  hgvsp: ENST00000540823.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34561G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*824C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.657C>T
  hgvsp: ENST00000397649.3:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52085
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys472Cys
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-24193009-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193009
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193009
    reference: chr 8
allele count: 3
allele frequency: 2.485871961021528e-5
allele num: 120682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.319G>T
  hgvsp: ENST00000521629.1:c.319G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34567C>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1422G>T
  hgvsp: ENST00000265769.4:c.1422G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1422G>T
  hgvsp: ENST00000437154.2:c.1422G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34567C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.723G>T
  hgvsp: ENST00000540823.1:c.723G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.663G>T
  hgvsp: ENST00000397649.3:c.663G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34567C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34567C>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*830G>T
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu474Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-24193013-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193013
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193013
    reference: chr 8
allele count: 1
allele frequency: 8.278282753025713e-6
allele num: 120798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.667G>C
  hgvsp: ENSP00000380770.3:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34571C>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*834G>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.323G>C
  hgvsp: ENSP00000429484.1:p.Glu109Gln
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34571C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1426G>C
  hgvsp: ENSP00000265769.4:p.Glu476Gln
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.727G>C
  hgvsp: ENSP00000443743.1:p.Glu243Gln
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1426G>C
  hgvsp: ENSP00000393699.2:p.Glu476Gln
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34571C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34571C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu476Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

8-24193027-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193027
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193027
    reference: chr 8
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1440T>C
  hgvsp: ENST00000437154.2:c.1440T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.741T>C
  hgvsp: ENST00000540823.1:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.681T>C
  hgvsp: ENST00000397649.3:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.337T>C
  hgvsp: ENST00000521629.1:c.337T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34585A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34585A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*848T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34585A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1440T>C
  hgvsp: ENST00000265769.4:c.1440T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34585A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly480Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

8-24193037-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193037
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193037
    reference: chr 8
allele count: 1
allele frequency: 8.316146630297385e-6
allele num: 120248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1450A>G
  hgvsp: ENSP00000393699.2:p.Asn484Asp
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.691A>G
  hgvsp: ENSP00000380770.3:p.Asn231Asp
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*858A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1450A>G
  hgvsp: ENSP00000265769.4:p.Asn484Asp
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.347A>G
  hgvsp: ENSP00000429484.1:p.Asn117Asp
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34595T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.751A>G
  hgvsp: ENSP00000443743.1:p.Asn251Asp
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34595T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34595T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34595T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn484Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

8-24193039-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193039
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193039
    reference: chr 8
allele count: 42
allele frequency: 3.493188282848446e-4
allele num: 120234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34597A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.753T>C
  hgvsp: ENST00000540823.1:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1452T>C
  hgvsp: ENST00000437154.2:c.1452T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.349T>C
  hgvsp: ENST00000521629.1:c.349T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1452T>C
  hgvsp: ENST00000265769.4:c.1452T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34597A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34597A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34597A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.693T>C
  hgvsp: ENST00000397649.3:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*860T>C
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44391
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10130
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn484Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

8-24193043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193043
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193043
    reference: chr 8
allele count: 1
allele frequency: 8.334583520861462e-6
allele num: 119982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.697C>T
  hgvsp: ENSP00000380770.3:p.Pro233Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34601G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1456C>T
  hgvsp: ENSP00000393699.2:p.Pro486Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34601G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34601G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.757C>T
  hgvsp: ENSP00000443743.1:p.Pro253Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34601G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1456C>T
  hgvsp: ENSP00000265769.4:p.Pro486Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*864C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.353C>T
  hgvsp: ENSP00000429484.1:p.Pro119Ser
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro486Ser
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

8-24193044-C-CTGATGATAGAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193044
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193055
    reference: chr 8
allele count: 1
allele frequency: 8.34125752798492e-6
allele num: 119886
alternate allele: CTGATGATAGAT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsp: ENSP00000429484.1:p.Phe123LeufsTer20
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsp: ENSP00000265769.4:p.Phe490LeufsTer20
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsp: ENSP00000380770.3:p.Phe237LeufsTer20
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsp: ENSP00000443743.1:p.Phe257LeufsTer20
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsp: ENSP00000393699.2:p.Phe490LeufsTer20
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe490LeufsTer20
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

8-24193050-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193050
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193050
    reference: chr 8
allele count: 1
allele frequency: 8.371983992766606e-6
allele num: 119446
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34608T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*871A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.764A>G
  hgvsp: ENSP00000443743.1:p.Asp255Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1463A>G
  hgvsp: ENSP00000265769.4:p.Asp488Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.360A>G
  hgvsp: ENSP00000429484.1:p.Asp121Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34608T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1463A>G
  hgvsp: ENSP00000393699.2:p.Asp488Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34608T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34608T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.704A>G
  hgvsp: ENSP00000380770.3:p.Asp235Gly
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49138
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp488Gly
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-24193051-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193051
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193051
    reference: chr 8
allele count: 1
allele frequency: 8.372264362619514e-6
allele num: 119442
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34609A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.765T>C
  hgvsp: ENST00000540823.1:c.765T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.705T>C
  hgvsp: ENST00000397649.3:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34609A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.361T>C
  hgvsp: ENST00000521629.1:c.361T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*872T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1464T>C
  hgvsp: ENST00000265769.4:c.1464T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34609A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34609A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1464T>C
  hgvsp: ENST00000437154.2:c.1464T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp488Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS

8-24193055-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193055
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193055
    reference: chr 8
allele count: 2
allele frequency: 1.681124335955887e-5
allele num: 118968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34613A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.709T>A
  hgvsp: ENSP00000380770.3:p.Phe237Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.769T>A
  hgvsp: ENSP00000443743.1:p.Phe257Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.365T>A
  hgvsp: ENSP00000429484.1:p.Phe123Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34613A>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*876T>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1468T>A
  hgvsp: ENSP00000393699.2:p.Phe490Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34613A>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1468T>A
  hgvsp: ENSP00000265769.4:p.Phe490Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34613A>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42215
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe490Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

8-24193065-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193065
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193065
    reference: chr 8
allele count: 531
allele frequency: 4.516304625172232e-3
allele num: 117574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.719A>G
  hgvsp: ENSP00000380770.3:p.Asn240Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1478A>G
  hgvsp: ENSP00000265769.4:p.Asn493Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.779A>G
  hgvsp: ENSP00000443743.1:p.Asn260Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34623T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34623T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.375A>G
  hgvsp: ENSP00000429484.1:p.Asn126Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1478A>G
  hgvsp: ENSP00000393699.2:p.Asn493Ser
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34623T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34623T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*886A>G
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 39909
  bin: 2.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9977
  bin: 2.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 9.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 9.75e1
  variant carriers: 512
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn493Ser
num of homozygotes: 11
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-24193066-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193066
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193066
    reference: chr 8
allele count: 1
allele frequency: 8.549346829902196e-6
allele num: 116968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34624A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.720T>C
  hgvsp: ENST00000397649.3:c.720T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.376T>C
  hgvsp: ENST00000521629.1:c.376T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34624A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1479T>C
  hgvsp: ENST00000437154.2:c.1479T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1479T>C
  hgvsp: ENST00000265769.4:c.1479T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34624A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.780T>C
  hgvsp: ENST00000540823.1:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*887T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34624A>G
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn493Asn
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

8-24193077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193077
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193077
    reference: chr 8
allele count: 3
allele frequency: 2.613923499172257e-5
allele num: 114770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1490G>A
  hgvsp: ENSP00000393699.2:p.Cys497Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.731G>A
  hgvsp: ENSP00000380770.3:p.Cys244Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.387G>A
  hgvsp: ENSP00000429484.1:p.Cys130Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34635C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.791G>A
  hgvsp: ENSP00000443743.1:p.Cys264Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1490G>A
  hgvsp: ENSP00000265769.4:p.Cys497Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*898G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34635C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34635C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34635C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10009
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36465
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5608
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys497Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-24193084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193084
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193084
    reference: chr 8
allele count: 1
allele frequency: 8.835483300936561e-6
allele num: 113180
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1497C>T
  hgvsp: ENST00000265769.4:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*905C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.738C>T
  hgvsp: ENST00000397649.3:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34642G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34642G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34642G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.394C>T
  hgvsp: ENST00000521629.1:c.394C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.798C>T
  hgvsp: ENST00000540823.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34642G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1497C>T
  hgvsp: ENST00000437154.2:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His499His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

8-24193085-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193085
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193085
    reference: chr 8
allele count: 325
allele frequency: 2.875648126847051e-3
allele num: 113018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34643C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.395G>A
  hgvsp: ENSP00000429484.1:p.Gly133Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34643C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1498G>A
  hgvsp: ENSP00000393699.2:p.Gly500Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1498G>A
  hgvsp: ENSP00000265769.4:p.Gly500Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.799G>A
  hgvsp: ENSP00000443743.1:p.Gly267Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34643C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34643C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*906G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.739G>A
  hgvsp: ENSP00000380770.3:p.Gly247Arg
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35288
  bin: 2.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Gly500Arg
num of homozygotes: 3
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

8-24193086-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193086
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193086
    reference: chr 8
allele count: 2
allele frequency: 1.772452542583172e-5
allele num: 112838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34644C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.396G>T
  hgvsp: ENSP00000429484.1:p.Gly133Val
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.740G>T
  hgvsp: ENSP00000380770.3:p.Gly247Val
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*907G>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34644C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1499G>T
  hgvsp: ENSP00000393699.2:p.Gly500Val
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1499G>T
  hgvsp: ENSP00000265769.4:p.Gly500Val
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.800G>T
  hgvsp: ENSP00000443743.1:p.Gly267Val
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34644C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34644C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40071
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly500Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-24193087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193087
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193087
    reference: chr 8
allele count: 1
allele frequency: 8.876895217128857e-6
allele num: 112652
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1500G>A
  hgvsp: ENST00000437154.2:c.1500G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.801G>A
  hgvsp: ENST00000540823.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34645C>T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34645C>T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.741G>A
  hgvsp: ENST00000397649.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34645C>T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34645C>T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*908G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1500G>A
  hgvsp: ENST00000265769.4:c.1500G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.397G>A
  hgvsp: ENST00000521629.1:c.397G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly500Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-24193089-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193089
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193089
    reference: chr 8
allele count: 1
allele frequency: 8.925065152975617e-6
allele num: 112044
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34647T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1502A>G
  hgvsp: ENSP00000393699.2:p.Lys501Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.743A>G
  hgvsp: ENSP00000380770.3:p.Lys248Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1502A>G
  hgvsp: ENSP00000265769.4:p.Lys501Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.803A>G
  hgvsp: ENSP00000443743.1:p.Lys268Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34647T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.399A>G
  hgvsp: ENSP00000429484.1:p.Lys134Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34647T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34647T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*910A>G
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys501Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

8-24193095-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193095
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193095
    reference: chr 8
allele count: 1
allele frequency: 9.075398409990198e-6
allele num: 110188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*916A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.809A>G
  hgvsp: ENSP00000443743.1:p.His270Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34653T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1508A>G
  hgvsp: ENSP00000265769.4:p.His503Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1508A>G
  hgvsp: ENSP00000393699.2:p.His503Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34653T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.405A>G
  hgvsp: ENSP00000429484.1:p.His136Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34653T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.749A>G
  hgvsp: ENSP00000380770.3:p.His250Arg
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34653T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His503Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

8-24193104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193104
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193104
    reference: chr 8
allele count: 3
allele frequency: 2.805154002954762e-5
allele num: 106946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*925T>C
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34662A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.758T>C
  hgvsp: ENSP00000380770.3:p.Met253Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1517T>C
  hgvsp: ENSP00000265769.4:p.Met506Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.414T>C
  hgvsp: ENSP00000429484.1:p.Met139Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34662A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.818T>C
  hgvsp: ENSP00000443743.1:p.Met273Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1517T>C
  hgvsp: ENSP00000393699.2:p.Met506Thr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34662A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34662A>G
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30670
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11872
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met506Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

8-24193105-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193105
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193105
    reference: chr 8
allele count: 3
allele frequency: 2.816055269778095e-5
allele num: 106532
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1518G>A
  hgvsp: ENSP00000265769.4:p.Met506Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.415G>A
  hgvsp: ENSP00000429484.1:p.Met139Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1518G>A
  hgvsp: ENSP00000393699.2:p.Met506Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*926G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34663C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34663C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.819G>A
  hgvsp: ENSP00000443743.1:p.Met273Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34663C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.759G>A
  hgvsp: ENSP00000380770.3:p.Met253Ile
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34663C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met506Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

8-24193113-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193113
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193112
    reference: chr 8
allele count: 1
allele frequency: 9.711755108383188e-6
allele num: 102968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34672delG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34672delG
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34672delG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34672delG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.771delC
  hgvsp: ENSP00000380770.3:p.Thr258HisfsTer69
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1530delC
  hgvsp: ENSP00000265769.4:p.Thr511HisfsTer69
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.427delC
  hgvsp: ENSP00000429484.1:p.Thr144HisfsTer69
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.831delC
  hgvsp: ENSP00000443743.1:p.Thr278HisfsTer34
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1530delC
  hgvsp: ENSP00000393699.2:p.Thr511HisfsTer34
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*938delC
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14847
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr511HisfsTer69
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: GC
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

8-24193117-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193117
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193117
    reference: chr 8
allele count: 1
allele frequency: 9.844457570387871e-6
allele num: 101580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34675G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34675G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.771C>T
  hgvsp: ENST00000397649.3:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1530C>T
  hgvsp: ENST00000265769.4:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*938C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.831C>T
  hgvsp: ENST00000540823.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.427C>T
  hgvsp: ENST00000521629.1:c.427C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1530C>T
  hgvsp: ENST00000437154.2:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34675G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34675G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro510Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

8-24193119-CACTGCAGGAGCAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193119
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193106
    reference: chr 8
allele count: 1
allele frequency: 9.950842836388241e-6
allele num: 100494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsp: ENSP00000265769.4:p.Leu512AlafsTer64
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsp: ENSP00000380770.3:p.Leu259AlafsTer64
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsp: ENSP00000443743.1:p.Leu279AlafsTer29
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsp: ENSP00000393699.2:p.Leu512AlafsTer29
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsp: ENSP00000429484.1:p.Leu145AlafsTer64
  variant of: http://identifiers.org/hgnc/206
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8902
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31079
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16843
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu512AlafsTer64
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: CACTGCAGGAGCAG
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-24193134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193134
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193134
    reference: chr 8
allele count: 1
allele frequency: 1.110420182997246e-5
allele num: 90056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34692C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34692C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.788G>A
  hgvsp: ENSP00000380770.3:p.Cys263Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34692C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*955G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1547G>A
  hgvsp: ENSP00000265769.4:p.Cys516Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.444G>A
  hgvsp: ENSP00000429484.1:p.Cys149Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.848G>A
  hgvsp: ENSP00000443743.1:p.Cys283Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1547G>A
  hgvsp: ENSP00000393699.2:p.Cys516Tyr
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34692C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys516Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

8-24193165-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193165
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193165
    reference: chr 8
allele count: 3
allele frequency: 4.799078576913232e-5
allele num: 62512
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1567+11A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*975+11A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34723T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.879A>G
  hgvsp: ENST00000540823.1:c.879A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34723T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34723T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.464+11A>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1578A>G
  hgvsp: ENST00000437154.2:c.1578A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34723T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.808+11A>G
  variant of: http://identifiers.org/hgnc/206
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19813
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr526Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

8-24193182-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193182
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193182
    reference: chr 8
allele count: 1
allele frequency: 2.500500100020004e-5
allele num: 39992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.808+28C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34740G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1567+28C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34740G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.896C>G
  hgvsp: ENSP00000443743.1:p.Ala299Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*975+28C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1595C>G
  hgvsp: ENSP00000393699.2:p.Ala532Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34740G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34740G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.464+28C>G
  variant of: http://identifiers.org/hgnc/206
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22899
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13379
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17542
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala532Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

8-24193188-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193188
    reference: chr 8
allele count: 1
allele frequency: 3.20225438708851e-5
allele num: 31228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1601C>G
  hgvsp: ENSP00000393699.2:p.Ala534Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1567+34C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34746G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34746G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.808+34C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.464+34C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.902C>G
  hgvsp: ENSP00000443743.1:p.Ala301Gly
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*975+34C>G
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34746G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34746G>C
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala534Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-24193188-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193188
    reference: chr 8
allele count: 271
allele frequency: 8.678109389009862e-3
allele num: 31228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.808+34C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34746G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34746G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1567+34C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34746G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.902C>T
  hgvsp: ENSP00000443743.1:p.Ala301Val
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*975+34C>T
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34746G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1601C>T
  hgvsp: ENSP00000393699.2:p.Ala534Val
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.464+34C>T
  variant of: http://identifiers.org/hgnc/206
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 1.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22238
  bin: 7.5e0
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21172
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 7.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala534Val
num of homozygotes: 3
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-24193189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193189
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193189
    reference: chr 8
allele count: 1
allele frequency: 3.352554646640741e-5
allele num: 29828
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34747C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34747C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*975+35G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1602G>A
  hgvsp: ENST00000437154.2:c.1602G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1567+35G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34747C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34747C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.808+35G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.903G>A
  hgvsp: ENST00000540823.1:c.903G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.464+35G>A
  variant of: http://identifiers.org/hgnc/206
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9088
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21993
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24824
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala534Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-24193193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24193193
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 24193193
    reference: chr 8
allele count: 2
allele frequency: 7.593014426727411e-5
allele num: 26340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000519689
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000519689.1:n.607-34751C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000430085
  ensembl transcript: ENST00000520448
  gene symbol: ADAM28
  hgvsc: ENST00000520448.1:c.*975+39G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000380770
  ensembl transcript: ENST00000397649
  gene symbol: ADAM28
  hgvsc: ENST00000397649.3:c.808+39G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000443743
  ensembl transcript: ENST00000540823
  gene symbol: ADAM28
  hgvsc: ENST00000540823.1:c.907G>A
  hgvsp: ENSP00000443743.1:p.Glu303Lys
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523578
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523578.1:n.502-34751C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000518988
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000518988.1:n.356-34751C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000393699
  ensembl transcript: ENST00000437154
  gene symbol: ADAM28
  hgvsc: ENST00000437154.2:c.1606G>A
  hgvsp: ENSP00000393699.2:p.Glu536Lys
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000265769
  ensembl transcript: ENST00000265769
  gene symbol: ADAM28
  hgvsc: ENST00000265769.4:c.1567+39G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042980
  ensembl protein: ENSP00000429484
  ensembl transcript: ENST00000521629
  gene symbol: ADAM28
  hgvsc: ENST00000521629.1:c.464+39G>A
  variant of: http://identifiers.org/hgnc/206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000253535
  ensembl transcript: ENST00000523700
  gene symbol: RP11-624C23.1
  hgvsc: ENST00000523700.1:n.165-34751C>T
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20650
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25284
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26188
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu536Lys
num of homozygotes: 0
reference allele: G

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

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

GenotypeQuality
all individuals: 8158
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2048
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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European (Finnish)
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QD
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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DP
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VQSLOD
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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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Latino
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South Asian
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European (Non-Finnish)
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Other
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African
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East Asian
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European (Finnish)
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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QD
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DP
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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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European (Non-Finnish)
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allele num: 66362
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Latino
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African
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European (Finnish)
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East Asian
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South Asian
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Other
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FS
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QD
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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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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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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FS
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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DP
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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QD
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FS
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SIO_000300: 2.643e0

MQ
type: SiteQuality
SIO_000300: 5.662e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.469e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64072
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9994
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South Asian
type: Population
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: 2.66998932004272e-4
allele num: 11236
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.86e-1

DP
type: SiteQuality
SIO_000300: 1.697577e6

FS
type: SiteQuality
SIO_000300: 1.2404e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8456
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 9.023641941887746e-5
allele num: 11082
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.800870511425463e-5
allele num: 14704
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.015847216578627e-4
allele num: 9844
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.596780889726312e-5
allele num: 62626
num of homozygotes: 0

Other
type: Population
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allele frequency: 1.187648456057007e-3
allele num: 842
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

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

BaseQRankSum
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SIO_000300: 1.11e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.674424835069154e-5
allele num: 59722
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10778
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.107e0

MQRankSum
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SIO_000300: -1.015e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

VQSLOD
type: SiteQuality
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.135e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 1.488e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.714442463310931e-5
allele num: 58328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13818
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6012
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

DP
type: SiteQuality
SIO_000300: 1.456457e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.832e1

FS
type: SiteQuality
SIO_000300: 2.886e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.513067953357459e-5
allele num: 39792
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3868
num of homozygotes: 0

South 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: 616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
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allele num: 544
num of homozygotes: 0

African
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allele count: 263
allele frequency: 4.693076374018558e-2
allele num: 5604
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European (Finnish)
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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: 15
allele frequency: 1.878287002253944e-3
allele num: 7986
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 5.878894767783657e-5
allele num: 34020
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East Asian
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allele count: 0
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South Asian
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allele count: 0
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

MQ
type: SiteQuality
SIO_000300: 5.714e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ReadPosRankSum
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ClippingRankSum
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DP
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FS
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MQRankSum
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VQSLOD
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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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South Asian
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allele frequency: 1.101564221194096e-4
allele num: 9078
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31252
num of homozygotes: 0

Latino
type: Population
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num of homozygotes: 0

Other
type: Population
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allele num: 522
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2572
num of homozygotes: 0

FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

ReadPosRankSum
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ClippingRankSum
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SIO_000300: 1.23e0

MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.823e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 4950
num of homozygotes: 0

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

East Asian
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allele frequency: 4.351610095735422e-4
allele num: 2298
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Other
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allele frequency: 0.0e0
allele num: 442
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European (Finnish)
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allele frequency: 0.0e0
allele num: 2232
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.659e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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DP
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QD
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BaseQRankSum
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SIO_000300: 1.95e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6822
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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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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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.694399290675336e-5
allele num: 27068
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.455e5

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

European (Non-Finnish)
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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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African
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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

Latino
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South Asian
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 41542
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South Asian
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Latino
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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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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South Asian
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allele frequency: 0.0e0
allele num: 6202
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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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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num of homozygotes: 0

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

African
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allele frequency: 7.158196134574087e-4
allele num: 8382
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Other
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DP
type: SiteQuality
SIO_000300: 8.65715e5

VQSLOD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.81e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -5.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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African
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num of homozygotes: 0

European (Finnish)
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allele frequency: 2.832326283987915e-3
allele num: 5296
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East Asian
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allele num: 5554
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Other
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European (Non-Finnish)
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allele frequency: 8.043910286741744e-4
allele num: 42268
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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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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East Asian
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num of homozygotes: 0

Other
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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MQRankSum
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FS
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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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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European (Non-Finnish)
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Latino
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African
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East Asian
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Other
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South Asian
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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QD
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InbreedingCoeff
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BaseQRankSum
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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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Latino
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South Asian
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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DP
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.089252883168979e-5
allele num: 47864
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.98e0

VQSLOD
type: SiteQuality
SIO_000300: -4.363e-1

DP
type: SiteQuality
SIO_000300: 1.099286e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.933e1

GenotypeQuality
all individuals: 13853
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 4.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.374867423498448e-4
allele num: 50914
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

FS
type: SiteQuality
SIO_000300: 1.036e0

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

DP
type: SiteQuality
SIO_000300: 1.173662e6

GenotypeQuality
all individuals: 518
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 195
bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 1439
bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 15

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
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variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 14
allele frequency: 2.037252619324796e-3
allele num: 6872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.210946960523129e-4
allele num: 8258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.964096319283498e-5
allele num: 50914
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.036e0

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 1.173662e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.537e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

FS
type: SiteQuality
SIO_000300: 1.036e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

DP
type: SiteQuality
SIO_000300: 1.173662e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeQuality
all individuals: 262
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.25e1
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GenotypeQuality
all individuals: 294
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GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 809
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variant carriers: 0

GenotypeQuality
all individuals: 483
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variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
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GenotypeQuality
all individuals: 1892
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variant carriers: 1

GenotypeQuality
all individuals: 113
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38332
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7596
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.080146899978397e-4
allele num: 9258
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.07e-1

DP
type: SiteQuality
SIO_000300: 1.265338e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.719e0

MQRankSum
type: SiteQuality
SIO_000300: 7.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 1.305e1

GenotypeQuality
all individuals: 2611
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
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GenotypeQuality
all individuals: 68
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GenotypeQuality
all individuals: 201
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GenotypeQuality
all individuals: 62
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GenotypeQuality
all individuals: 537
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GenotypeQuality
all individuals: 1889
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 199
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variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.232134056185313e-4
allele num: 8116
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10914
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59914
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.605e1

DP
type: SiteQuality
SIO_000300: 1.337242e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: -9.187e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.981e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
all individuals: 2623
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.926543577526305e-5
allele num: 10074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60436
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.449779519843214e-4
allele num: 8164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.006e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

VQSLOD
type: SiteQuality
SIO_000300: -1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

FS
type: SiteQuality
SIO_000300: 8.864000000000001e0

DP
type: SiteQuality
SIO_000300: 1.346435e6

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
SIO_000300: 7.89e0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 331
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 562
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variant carriers: 0

GenotypeQuality
all individuals: 49264
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64480
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.590708972218005e-5
allele num: 13174
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.69e1

FS
type: SiteQuality
SIO_000300: 3.042e0

DP
type: SiteQuality
SIO_000300: 1.423869e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.193e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.56e-1

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 189
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1893
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GenotypeQuality
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GenotypeQuality
all individuals: 157
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GenotypeQuality
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 581
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GenotypeQuality
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GenotypeQuality
all individuals: 203
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 632
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13724
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53955106690889e-5
allele num: 64954
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.88e-1

FS
type: SiteQuality
SIO_000300: 5.632e0

DP
type: SiteQuality
SIO_000300: 1.434898e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.013e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.844564682734874e-4
allele num: 65056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 30
allele frequency: 4.557885141294439e-3
allele num: 6582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

DP
type: SiteQuality
SIO_000300: 1.437936e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

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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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053248656570591e-5
allele num: 65504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14568
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.251e0

MQRankSum
type: SiteQuality
SIO_000300: -4.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

FS
type: SiteQuality
SIO_000300: 4.02e-1

QD
type: SiteQuality
SIO_000300: 1.151e1

DP
type: SiteQuality
SIO_000300: 1.450251e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.71591672263264e-5
allele num: 14890
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520958812435359e-5
allele num: 65748
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.369e0

QD
type: SiteQuality
SIO_000300: 1.047e1

DP
type: SiteQuality
SIO_000300: 1.456415e6

GenotypeQuality
all individuals: 11
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512264464809606e-5
allele num: 66126
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.06e-1

FS
type: SiteQuality
SIO_000300: 2.684e0

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

DP
type: SiteQuality
SIO_000300: 1.468483e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

QD
type: SiteQuality
SIO_000300: 1.574e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.343e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016773259321829e-5
allele num: 66296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15966
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

QD
type: SiteQuality
SIO_000300: 1.149e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.1119e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

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

VQSLOD
type: SiteQuality
SIO_000300: -9.782999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.477563e6

GenotypeQuality
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variant carriers: 0

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

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: 6608
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 3
allele frequency: 2.59920291110726e-4
allele num: 11542
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.218e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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

BaseQRankSum
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SIO_000300: -2.601e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66416
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.947e-1

QD
type: SiteQuality
SIO_000300: 1.449e1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66302
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.476e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.259e0

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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bin: 1.25e1
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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: 300
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GenotypeQuality
all individuals: 234
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
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: 6574
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.153846153846154e-5
allele num: 16250
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.387e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

DP
type: SiteQuality
SIO_000300: 1.472744e6

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

European (Non-Finnish)
type: Population
allele count: 39
allele frequency: 5.903009021008658e-4
allele num: 66068
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.521606816798539e-4
allele num: 6572
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.156119182467373e-5
allele num: 16244
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.369e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

DP
type: SiteQuality
SIO_000300: 1.473037e6

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
all individuals: 1191
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GenotypeQuality
all individuals: 653
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.167133520074697e-4
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65916
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.875e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.468363e6

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518372304889159e-5
allele num: 65860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.456e0

MQ
type: SiteQuality
SIO_000300: 5.104e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-2

DP
type: SiteQuality
SIO_000300: 1.467396e6

QD
type: SiteQuality
SIO_000300: 4.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

VQSLOD
type: SiteQuality
SIO_000300: -2.839e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.086e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16082
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65618
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.756567425569177e-5
allele num: 11420
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 3.354e0

QD
type: SiteQuality
SIO_000300: 9.93e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: -1.033e0

DP
type: SiteQuality
SIO_000300: 1.459207e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.704e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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: 8552
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.218132073125233e-5
allele num: 16082
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 7.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.763e1

BaseQRankSum
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SIO_000300: 3.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.786e0

VQSLOD
type: SiteQuality
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FS
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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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: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
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South Asian
type: Population
allele count: 2
allele frequency: 1.25093820365274e-4
allele num: 15988
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6494
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.381e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.3e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

MQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

DP
type: SiteQuality
SIO_000300: 1.452127e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.55e-1

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 285
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GenotypeQuality
all individuals: 3117
bin: 6.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.292816652727442e-5
allele num: 64566
num of homozygotes: 0

Latino
type: Population
allele count: 27
allele frequency: 2.396166134185303e-3
allele num: 11268
num of homozygotes: 0

African
type: Population
allele count: 497
allele frequency: 4.855412270418132e-2
allele num: 10236
num of homozygotes: 11

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.334726973267453e-5
allele num: 15786
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.446308e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.49e-2

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: 3.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15712
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556807921038702e-5
allele num: 64234
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.428499e6

MQ
type: SiteQuality
SIO_000300: 5.901e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

FS
type: SiteQuality
SIO_000300: 1.9319e1

VQSLOD
type: SiteQuality
SIO_000300: -2.829e0

MQRankSum
type: SiteQuality
SIO_000300: 8.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.149e0

QD
type: SiteQuality
SIO_000300: 9.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.43e-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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11024
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.989238740534077e-4
allele num: 10036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15428
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.208e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.234e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.400937e6

QD
type: SiteQuality
SIO_000300: 1.232e1

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
all individuals: 1916
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variant carriers: 1

GenotypeQuality
all individuals: 1208
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.61087663906698e-5
allele num: 62078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.113e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.117e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 2.666e0

DP
type: SiteQuality
SIO_000300: 1.382243e6

QD
type: SiteQuality
SIO_000300: 1.875e1

GenotypeQuality
all individuals: 1167
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variant carriers: 0

GenotypeQuality
all individuals: 270
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 315

GenotypeQuality
all individuals: 39771
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GenotypeQuality
all individuals: 543
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 11
allele frequency: 1.014385835485061e-3
allele num: 10844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 208
allele frequency: 3.354622282433392e-3
allele num: 62004
num of homozygotes: 0

South Asian
type: Population
allele count: 86
allele frequency: 5.654918463966333e-3
allele num: 15208
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.152832674571805e-3
allele num: 6072
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.110886689557665e-3
allele num: 9902
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.380952380952381e-3
allele num: 840
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.426e1

DP
type: SiteQuality
SIO_000300: 1.386644e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 517
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GenotypeQuality
all individuals: 1913
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.231226573607342e-5
allele num: 61896
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.416e0

MQRankSum
type: SiteQuality
SIO_000300: -2.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.804e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.37829e6

QD
type: SiteQuality
SIO_000300: 5.4e0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 204
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.281603861147207e-5
allele num: 10774
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61818
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 1.374976e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.134e0

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 4.499e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.602e1

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
all individuals: 520
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GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.193317422434368e-3
allele num: 838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15074
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.365154e6

FS
type: SiteQuality
SIO_000300: 9.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.9e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 3.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.137e0

QD
type: SiteQuality
SIO_000300: 1.231e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

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
all individuals: 2709
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GenotypeQuality
all individuals: 1388
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5878
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60424
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.744907594765952e-5
allele num: 14826
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: -1.455e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.342642e6

ReadPosRankSum
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SIO_000300: 1.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

QD
type: SiteQuality
SIO_000300: 1.472e1

MQRankSum
type: SiteQuality
SIO_000300: 8.05e-1

MQ
type: SiteQuality
SIO_000300: 5.79e1

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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bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
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allele frequency: 2.098489087856743e-4
allele num: 14296
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 58630
num of homozygotes: 0

Other
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num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.412e0

VQSLOD
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MQ
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InbreedingCoeff
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SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.267e0

FS
type: SiteQuality
SIO_000300: 2.0416e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.78e-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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variant carriers: 0

East Asian
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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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5666
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 5.137338173847524e-5
allele num: 58396
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -3.8e-2

QD
type: SiteQuality
SIO_000300: 1.385e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9782
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7396
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.771479185119575e-5
allele num: 56450
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 13726
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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SIO_000300: 1.5e0

MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 55700
num of homozygotes: 0

African
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allele frequency: 1.079214331966328e-4
allele num: 9266
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9638
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.746e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 55142
num of homozygotes: 0

Other
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num of homozygotes: 0

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

East Asian
type: Population
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 49448
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South Asian
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African
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BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Other
type: Population
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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South Asian
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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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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variant carriers: 0

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

East Asian
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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African
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South Asian
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Other
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ClippingRankSum
type: SiteQuality
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DP
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.195e1

GenotypeQuality
all individuals: 484
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24865
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 783
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22096
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2020
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17790
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.216312056737589e-4
allele num: 4512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2084
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.02279e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.54e-2

QD
type: SiteQuality
SIO_000300: 1.315e1

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1221
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 244
bin: 8.25e1
variant carriers: 22

GenotypeQuality
all individuals: 24865
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 21

GenotypeQuality
all individuals: 2062
bin: 9.75e1
variant carriers: 274

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 640
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 22096
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 2639
bin: 1.75e1
variant carriers: 10

GenotypeQuality
all individuals: 208
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 484
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 8

African
type: Population
allele count: 258
allele frequency: 5.718085106382979e-2
allele num: 4512
num of homozygotes: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17790
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 4.798464491362764e-3
allele num: 2084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1406
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 9.541984732824427e-4
allele num: 3144
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

DP
type: SiteQuality
SIO_000300: 6.02279e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

QD
type: SiteQuality
SIO_000300: 1.315e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.54e-2

GenotypeQuality
all individuals: 23164
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1823
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4262
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.306878306878307e-4
allele num: 3024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.26e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.86172e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 5.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

VQSLOD
type: SiteQuality
SIO_000300: -1.883e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0