7-24784313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784313
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784313
    reference: chr 7
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.292C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-221C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.272C>T
  hgvsp: ENSP00000339587.3:p.Thr91Ile
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.41C>T
  hgvsp: ENSP00000414090.2:p.Thr14Ile
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-221C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-221C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.272C>T
  hgvsp: ENSP00000386670.3:p.Thr91Ile
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-221C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.291C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25533
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr91Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-24784321-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784321
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784321
    reference: chr 7
allele count: 1
allele frequency: 8.292836647703714e-6
allele num: 120586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-229G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-229G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.283G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-229G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.33G>T
  hgvsp: ENST00000411476.2:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.264G>T
  hgvsp: ENST00000342947.3:c.264G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.264G>T
  hgvsp: ENST00000409775.3:c.264G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.284G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-229G>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val88Val
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-24784324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784324
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784324
    reference: chr 7
allele count: 1
allele frequency: 8.29462508294625e-6
allele num: 120560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.261C>T
  hgvsp: ENST00000409775.3:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-232C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-232C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.30C>T
  hgvsp: ENST00000411476.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.281C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.261C>T
  hgvsp: ENST00000342947.3:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-232C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.280C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-232C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His87His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

7-24784327-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784327
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784327
    reference: chr 7
allele count: 1
allele frequency: 8.296827293243064e-6
allele num: 120528
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-235C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-235C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.258C>G
  hgvsp: ENSP00000386670.3:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.278C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.277C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-235C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-235C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.27C>G
  hgvsp: ENSP00000414090.2:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.258C>G
  hgvsp: ENSP00000339587.3:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10602
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn86Lys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

7-24784329-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784329
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784329
    reference: chr 7
allele count: 2
allele frequency: 1.659723490066555e-5
allele num: 120502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.256A>C
  hgvsp: ENSP00000386670.3:p.Asn86His
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.25A>C
  hgvsp: ENSP00000414090.2:p.Asn9His
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-237A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.276A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-237A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.275A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.256A>C
  hgvsp: ENSP00000339587.3:p.Asn86His
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-237A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-237A>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9374
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25439
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn86His
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/7-24784336-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784336
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784336
    reference: chr 7
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.18G>T
  hgvsp: ENSP00000414090.2:p.Lys6Asn
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.249G>T
  hgvsp: ENSP00000386670.3:p.Lys83Asn
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.269G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-244G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-244G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-244G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-244G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.249G>T
  hgvsp: ENSP00000339587.3:p.Lys83Asn
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.268G>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4542
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9353
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys83Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

7-24784338-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784338
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784338
    reference: chr 7
allele count: 9
allele frequency: 7.475703962123099e-5
allele num: 120390
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.247A>G
  hgvsp: ENSP00000339587.3:p.Lys83Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.247A>G
  hgvsp: ENSP00000386670.3:p.Lys83Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-246A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.16A>G
  hgvsp: ENSP00000414090.2:p.Lys6Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-246A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.267A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-246A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-246A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.266A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys83Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

7-24784344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784344
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784344
    reference: chr 7
allele count: 1
allele frequency: 8.309788931361144e-6
allele num: 120340
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.241G>A
  hgvsp: ENSP00000339587.3:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.261G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-252G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-252G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.241G>A
  hgvsp: ENSP00000386670.3:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-252G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000414090
  ensembl transcript: ENST00000411476
  gene symbol: DFNA5
  hgvsc: ENST00000411476.2:c.10G>A
  hgvsp: ENSP00000414090.2:p.Glu4Lys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.260G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-252G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3428
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu81Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

7-24784355-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784355
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784355
    reference: chr 7
allele count: 1
allele frequency: 8.320990530712775e-6
allele num: 120178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-263T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.230T>C
  hgvsp: ENSP00000386670.3:p.Phe77Ser
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-263T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-263T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.250T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-263T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.230T>C
  hgvsp: ENSP00000339587.3:p.Phe77Ser
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.249T>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15459
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10560
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe77Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

7-24784360-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784360
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784360
    reference: chr 7
allele count: 4
allele frequency: 3.332888948140248e-5
allele num: 120016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.245G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.244G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-268G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.225G>A
  hgvsp: ENST00000342947.3:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-268G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-268G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.225G>A
  hgvsp: ENST00000409775.3:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-268G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24607
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3369
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser75Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

7-24784361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784361
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784361
    reference: chr 7
allele count: 3
allele frequency: 2.499833344443704e-5
allele num: 120008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.224C>T
  hgvsp: ENSP00000386670.3:p.Ser75Leu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-269C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.244C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-269C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-269C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-269C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.224C>T
  hgvsp: ENSP00000339587.3:p.Ser75Leu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.243C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9117
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3362
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser75Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

7-24784368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784368
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784368
    reference: chr 7
allele count: 1
allele frequency: 8.339031671642289e-6
allele num: 119918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-276G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.236G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-276G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.237G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.217G>A
  hgvsp: ENSP00000386670.3:p.Val73Met
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-276G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.217G>A
  hgvsp: ENSP00000339587.3:p.Val73Met
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-276G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15050
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val73Met
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

7-24784369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784369
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784369
    reference: chr 7
allele count: 2
allele frequency: 1.668084538524412e-5
allele num: 119898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.235C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-277C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.216C>T
  hgvsp: ENST00000409775.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-277C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-277C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.216C>T
  hgvsp: ENST00000342947.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-277C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.236C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14982
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3088
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val72Val
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

7-24784375-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784375
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784375
    reference: chr 7
allele count: 1
allele frequency: 8.349475652928997e-6
allele num: 119768
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-2A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-2A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-2A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-2A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-2A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-2A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-2A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-2A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3044
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4305
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10501
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 8.75e1
  variant carriers: 0
hgvs: c.212-2A>G
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-24784380-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784380
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784380
    reference: chr 7
allele count: 1
allele frequency: 8.358688020328329e-6
allele num: 119636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-7A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-7A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-7A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-7A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-7A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-7A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-7A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-7A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 9.25e1
  variant carriers: 0
hgvs: c.212-7A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

7-24784387-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784387
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784387
    reference: chr 7
allele count: 6
allele frequency: 5.028326237806309e-5
allele num: 119324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-14C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-14C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-14C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-14C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-14C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-14C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-14C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-14C>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16883
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2955
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

7-24784388-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784388
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784388
    reference: chr 7
allele count: 1
allele frequency: 8.379139294811638e-6
allele num: 119344
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-15T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-15T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-15T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-15T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-15T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-15T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-15T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-15T>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2995
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2956
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/7-24784389-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784389
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784389
    reference: chr 7
allele count: 1
allele frequency: 8.38841727342885e-6
allele num: 119212
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-16G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-16G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-16G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-16G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-16G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-16G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-16G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-16G>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

7-24784389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784389
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784389
    reference: chr 7
allele count: 4
allele frequency: 3.35536690937154e-5
allele num: 119212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-16G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-16G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-16G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-16G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-16G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-16G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-16G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-16G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7731
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-24784390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784390
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784390
    reference: chr 7
allele count: 46
allele frequency: 3.859837551184802e-4
allele num: 119176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-17C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-17C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-17C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-17C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-17C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-17C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-17C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-17C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12879
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16148
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 3.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 19246
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4029
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

7-24784394-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784394
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784394
    reference: chr 7
allele count: 1
allele frequency: 8.415949908266146e-6
allele num: 118822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-21T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-21T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-21T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-21T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-21T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-21T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-21T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-21T>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14328
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2886
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2583
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-24784395-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784395
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784395
    reference: chr 7
allele count: 4
allele frequency: 3.369442525734117e-5
allele num: 118714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-22C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-22C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-22C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-22C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-22C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-22C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-22C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-22C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2833
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

7-24784398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784398
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784398
    reference: chr 7
allele count: 8
allele frequency: 6.761668103521139e-5
allele num: 118314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-25C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-25C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-25C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-25C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-25C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-25C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-25C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-25C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9985
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2907
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12195
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

7-24784402-CCGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784402
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784399
    reference: chr 7
allele count: 223
allele frequency: 2.912519917456835e-3
allele num: 76566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-32_-281-30delTCG
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-32_-281-30delTCG
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-32_212-30delTCG
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-32_212-30delTCG
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-32_-281-30delTCG
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-32_232-30delTCG
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-32_231-30delTCG
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-32_-281-30delTCG
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9344
  bin: 2.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 1.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 13289
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 9574
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 4.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 19158
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1538
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8894
  bin: 9.75e1
  variant carriers: 220
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 3
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: CCGA
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

7-24784403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784403
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784403
    reference: chr 7
allele count: 69042
allele frequency: 5.8760149108921e-1
allele num: 117498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-30G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-30G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-30G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-30G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-30G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-30G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-30G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-30G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 8987
  bin: 3.25e1
  variant carriers: 7772
genotype depth: GenotypeDepth
  all individuals: 13043
  bin: 2.75e1
  variant carriers: 9540
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 277
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.75e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 1.75e1
  variant carriers: 5037
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 4.25e1
  variant carriers: 2518
genotype depth: GenotypeDepth
  all individuals: 9871
  bin: 2.25e1
  variant carriers: 8316
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 3.75e1
  variant carriers: 4812
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 5.25e1
  variant carriers: 686
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 1225
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 1.25e1
  variant carriers: 1734
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 7.5e0
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 9.75e1
  variant carriers: 4642
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 414
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 3.75e1
  variant carriers: 475
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 1.25e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 8.75e1
  variant carriers: 877
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 9.25e1
  variant carriers: 1494
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 2.25e1
  variant carriers: 230
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.5e0
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 7.5e0
  variant carriers: 105
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 7.75e1
  variant carriers: 1650
num of homozygotes: 21537
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/7-24784405-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784405
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784405
    reference: chr 7
allele count: 1
allele frequency: 1.320445782496171e-5
allele num: 75732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-32T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-32T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-32T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-32T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-32T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-32T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-32T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-32T>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7772
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18586
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6218
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-24784406-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784406
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784406
    reference: chr 7
allele count: 718
allele frequency: 9.463805557020087e-3
allele num: 75868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-33A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-33A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-33A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-33A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-33A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-33A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-33A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-33A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 3.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 2.25e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 15125
  bin: 2.75e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 1.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 3302
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18678
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4678
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6818
  bin: 9.75e1
  variant carriers: 706
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 6
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

7-24784420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24784420
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24784420
    reference: chr 7
allele count: 14
allele frequency: 1.239574294770767e-4
allele num: 112942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.232-47G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.212-47G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-281-47G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-47G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-47G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.212-47G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.231-47G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-47G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10989
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11826
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16511
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7084
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8111
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

7-24789132-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789132
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789132
    reference: chr 7
allele count: 2
allele frequency: 1.671541997492687e-5
allele num: 119650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4759T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+51T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+51T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4759T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+51T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4759T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+51T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+51T>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8987
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4477
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10989
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2401
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

7-24789133-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789133
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789132
    reference: chr 7
allele count: 2
allele frequency: 1.680954782316356e-5
allele num: 118980
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+49delC
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4761delC
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+49delC
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+49delC
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4761delC
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+49delC
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4761delC
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+49delC
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8871
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: AG
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

7-24789135-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789135
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789135
    reference: chr 7
allele count: 1
allele frequency: 8.945343948474819e-6
allele num: 111790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+48C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4762C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+48C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4762C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+48C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4762C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+48C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+48C>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3579
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8355
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

7-24789144-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789144
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789144
    reference: chr 7
allele count: 1
allele frequency: 8.334861391255063e-6
allele num: 119978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4771A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+39A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+39A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+39A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+39A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+39A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4771A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4771A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22432
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4216
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9280
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

7-24789147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789147
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789147
    reference: chr 7
allele count: 4
allele frequency: 3.33205604518268e-5
allele num: 120046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4774G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+36G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+36G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+36G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+36G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+36G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4774G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4774G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9284
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

7-24789148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789148
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789148
    reference: chr 7
allele count: 1
allele frequency: 8.326117364950376e-6
allele num: 120104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+35C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+35C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4775C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+35C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+35C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+35C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4775C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4775C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13995
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22650
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9587
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

7-24789148-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789148
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789148
    reference: chr 7
allele count: 530
allele frequency: 4.412842203423699e-3
allele num: 120104
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+35C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4775C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+35C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+35C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+35C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+35C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4775C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4775C>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 13995
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 15405
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 3946
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9587
  bin: 9.75e1
  variant carriers: 516
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 12
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

7-24789154-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789154
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789154
    reference: chr 7
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4781T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+29T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+29T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4781T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4781T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+29T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+29T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+29T>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23160
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

7-24789156-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789156
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789156
    reference: chr 7
allele count: 1
allele frequency: 8.308408109006315e-6
allele num: 120360
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+27A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4783A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4783A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+27A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+27A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+27A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+27A>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4783A>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9310
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9171
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

7-24789158-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789158
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789158
    reference: chr 7
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4785T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+25T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+25T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+25T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+25T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4785T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4785T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+25T>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5162
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-24789178-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789178
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789178
    reference: chr 7
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+5G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4805G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+5G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4805G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+5G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4805G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+5G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+5G>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9188
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23647
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
hgvs: c.211+5G>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-24789179-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789179
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789179
    reference: chr 7
allele count: 2
allele frequency: 1.653111155194075e-5
allele num: 120984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4806T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282+4T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4806T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230+4T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211+4T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211+4T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231+4T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4806T>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14304
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23684
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
hgvs: c.211+4T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

7-24789183-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789183
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789183
    reference: chr 7
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.211G>C
  hgvsp: ENSP00000339587.3:p.Val71Leu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.211G>C
  hgvsp: ENSP00000386670.3:p.Val71Leu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.231G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4810G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.230G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4810G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-282G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4810G>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val71Leu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

7-24789191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789191
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789191
    reference: chr 7
allele count: 3
allele frequency: 2.47618733182561e-5
allele num: 121154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4818C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4818C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-290C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.203C>T
  hgvsp: ENSP00000339587.3:p.Pro68Leu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4818C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.203C>T
  hgvsp: ENSP00000386670.3:p.Pro68Leu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.222C>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.223C>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5184
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro68Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-24789196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789196
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789196
    reference: chr 7
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4823A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4823A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4823A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.198A>G
  hgvsp: ENST00000409775.3:c.198A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.198A>G
  hgvsp: ENST00000342947.3:c.198A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.218A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.217A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-295A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9351
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln66Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

7-24789201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789201
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789201
    reference: chr 7
allele count: 3
allele frequency: 2.474471700291988e-5
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4828G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.193G>A
  hgvsp: ENSP00000386670.3:p.Asp65Asn
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.193G>A
  hgvsp: ENSP00000339587.3:p.Asp65Asn
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4828G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4828G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.212G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-300G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.213G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4015
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9189
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp65Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-24789206-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789206
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789206
    reference: chr 7
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.188T>C
  hgvsp: ENSP00000339587.3:p.Ile63Thr
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.188T>C
  hgvsp: ENSP00000386670.3:p.Ile63Thr
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4833T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-305T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4833T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.208T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4833T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.207T>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15592
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4016
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5190
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile63Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/7-24789214-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789214
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789214
    reference: chr 7
allele count: 3
allele frequency: 2.473043822336532e-5
allele num: 121308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-313T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.180T>G
  hgvsp: ENSP00000339587.3:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.180T>G
  hgvsp: ENSP00000386670.3:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4841T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.199T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.200T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4841T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4841T>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23830
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4229
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp60Glu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

7-24789215-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789215
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789215
    reference: chr 7
allele count: 4
allele frequency: 3.29733740004946e-5
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.179A>G
  hgvsp: ENSP00000386670.3:p.Asp60Gly
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.199A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-314A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.198A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.179A>G
  hgvsp: ENSP00000339587.3:p.Asp60Gly
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4842A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4842A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4842A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp60Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

7-24789216-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789216
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789216
    reference: chr 7
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.178G>A
  hgvsp: ENSP00000386670.3:p.Asp60Asn
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.178G>A
  hgvsp: ENSP00000339587.3:p.Asp60Asn
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4843G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.198G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-315G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.197G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4843G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4843G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4014
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp60Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

7-24789219-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789219
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789219
    reference: chr 7
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4846G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.175G>A
  hgvsp: ENSP00000339587.3:p.Gly59Ser
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4846G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.195G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-318G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4846G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.194G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.175G>A
  hgvsp: ENSP00000386670.3:p.Gly59Ser
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9186
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly59Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

7-24789249-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789249
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789249
    reference: chr 7
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4876C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.145C>A
  hgvsp: ENSP00000339587.3:p.Pro49Thr
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.145C>A
  hgvsp: ENSP00000386670.3:p.Pro49Thr
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.164C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.165C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-348C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4876C>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4876C>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro49Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-24789251-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789251
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789251
    reference: chr 7
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-350G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4878G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4878G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.143G>T
  hgvsp: ENSP00000339587.3:p.Arg48Ile
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.162G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.143G>T
  hgvsp: ENSP00000386670.3:p.Arg48Ile
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.163G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4878G>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg48Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

7-24789255-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789255
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789255
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.159C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.139C>G
  hgvsp: ENSP00000339587.3:p.Gln47Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4882C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-354C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.158C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4882C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4882C>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.139C>G
  hgvsp: ENSP00000386670.3:p.Gln47Glu
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4227
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln47Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-24789256-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789256
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789256
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4883G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.157G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.158G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.138G>T
  hgvsp: ENSP00000339587.3:p.Trp46Cys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4883G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.138G>T
  hgvsp: ENSP00000386670.3:p.Trp46Cys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-355G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4883G>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9185
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp46Cys
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-24789261-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789261
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789261
    reference: chr 7
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.133T>A
  hgvsp: ENSP00000339587.3:p.Cys45Ser
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.152T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.133T>A
  hgvsp: ENSP00000386670.3:p.Cys45Ser
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-360T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.153T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4888T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4888T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4888T>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys45Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

7-24789262-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789262
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789262
    reference: chr 7
allele count: 6
allele frequency: 4.94274651948266e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.132G>C
  hgvsp: ENSP00000386670.3:p.Trp44Cys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.151G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.152G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-361G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4889G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4889G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4889G>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.132G>C
  hgvsp: ENSP00000339587.3:p.Trp44Cys
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4015
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9366
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Trp44Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

7-24789269-CTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789269
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789266
    reference: chr 7
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.122_124delAGA
  hgvsp: ENSP00000339587.3:p.Lys41del
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4899_-281-4897delAGA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.142_144delAGA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4899_-281-4897delAGA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.122_124delAGA
  hgvsp: ENSP00000386670.3:p.Lys41del
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-371_-369delAGA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4899_-281-4897delAGA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.141_143delAGA
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23894
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4227
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys41del
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: CTCT
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-24789272-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789272
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789272
    reference: chr 7
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.122A>G
  hgvsp: ENSP00000386670.3:p.Lys41Arg
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.142A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-371A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.122A>G
  hgvsp: ENSP00000339587.3:p.Lys41Arg
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.141A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4899A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4899A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4899A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23889
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys41Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-24789274-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789274
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789275
    reference: chr 7
allele count: 138
allele frequency: 1.13677551154898e-3
allele num: 121396
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.139dupA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.138dupA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4902dupA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4902dupA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.119dupA
  hgvsp: ENSP00000386670.3:p.Lys41GlufsTer113
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-374dupA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4902dupA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.119dupA
  hgvsp: ENSP00000339587.3:p.Lys41GlufsTer113
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.75e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9352
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys41GlufsTer113
num of homozygotes: 1
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-24789274-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789274
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789273
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.119delA
  hgvsp: ENSP00000339587.3:p.Lys40ArgfsTer24
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4902delA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4902delA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4902delA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.119delA
  hgvsp: ENSP00000386670.3:p.Lys40ArgfsTer24
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.139delA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-374delA
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.138delA
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys40ArgfsTer24
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: CT
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

7-24789274-CTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789274
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789270
    reference: chr 7
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4217
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9352
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9252
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 23881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11576
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 2
  allele frequency: 2.313208420078649e-4
  allele num: 8646
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6614
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10404
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: CTTTT
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

7-24789280-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789280
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789280
    reference: chr 7
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-379A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.114A>G
  hgvsp: ENST00000342947.3:c.114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.114A>G
  hgvsp: ENST00000409775.3:c.114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4907A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.133A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4907A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.134A>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4907A>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23936
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr38Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

7-24789292-T-TATCAGAAGCTGTAACTTTAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789292
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789312
    reference: chr 7
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: TATCAGAAGCTGTAACTTTAC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsp: ENSP00000386670.3:p.Ser35Ter
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsp: ENSP00000339587.3:p.Ser35Ter
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 14446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9152
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser35Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

7-24789304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789304
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789304
    reference: chr 7
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4931G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.90G>A
  hgvsp: ENST00000342947.3:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4931G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.110G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.90G>A
  hgvsp: ENST00000409775.3:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.109G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4931G>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-403G>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4230
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9364
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys30Lys
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/7-24789307-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789307
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789307
    reference: chr 7
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4934T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4934T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.87T>G
  hgvsp: ENSP00000339587.3:p.Asp29Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-406T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.87T>G
  hgvsp: ENSP00000386670.3:p.Asp29Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.107T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.106T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4934T>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23895
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4001
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp29Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

7-24789307-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789307
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789307
    reference: chr 7
allele count: 182
allele frequency: 1.499200975304371e-3
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.87T>A
  hgvsp: ENSP00000386670.3:p.Asp29Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.87T>A
  hgvsp: ENSP00000339587.3:p.Asp29Glu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4934T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4934T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-406T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4934T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.107T>A
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.106T>A
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15588
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp29Glu
num of homozygotes: 2
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-24789316-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789316
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789316
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.78T>G
  hgvsp: ENSP00000339587.3:p.Asn26Lys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-415T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.78T>G
  hgvsp: ENSP00000386670.3:p.Asn26Lys
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.97T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4943T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.98T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4943T>G
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4943T>G
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4013
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4231
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9109
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn26Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-24789316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789316
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789316
    reference: chr 7
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4943T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4943T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.98T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.78T>C
  hgvsp: ENST00000342947.3:c.78T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.97T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.78T>C
  hgvsp: ENST00000409775.3:c.78T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-415T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4943T>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4231
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn26Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/7-24789319-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789319
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789319
    reference: chr 7
allele count: 6
allele frequency: 4.942502224126001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.94G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4946G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4946G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.75G>T
  hgvsp: ENST00000409775.3:c.75G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-418G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.75G>T
  hgvsp: ENST00000342947.3:c.75G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4946G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.95G>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4013
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23948
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu25Leu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/7-24789330-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789330
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789330
    reference: chr 7
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.83G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.64G>T
  hgvsp: ENSP00000339587.3:p.Val22Leu
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4957G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.84G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-429G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4957G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4957G>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.64G>T
  hgvsp: ENSP00000386670.3:p.Val22Leu
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9374
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4012
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5186
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val22Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

7-24789335-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789335
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789335
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4962T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-434T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.59T>C
  hgvsp: ENSP00000386670.3:p.Ile20Thr
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.78T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4962T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.79T>C
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.59T>C
  hgvsp: ENSP00000339587.3:p.Ile20Thr
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4962T>C
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23932
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4231
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile20Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

7-24789347-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24789347
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 24789347
    reference: chr 7
allele count: 4
allele frequency: 3.296467834715103e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000339587
  ensembl transcript: ENST00000342947
  gene symbol: DFNA5
  hgvsc: ENST00000342947.3:c.47A>T
  hgvsp: ENSP00000339587.3:p.Asp16Val
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000387119
  ensembl transcript: ENST00000409970
  gene symbol: DFNA5
  hgvsc: ENST00000409970.1:c.-281-4974A>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000442661
  ensembl transcript: ENST00000545231
  gene symbol: DFNA5
  hgvsc: ENST00000545231.1:c.-446A>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000401332
  ensembl transcript: ENST00000419307
  gene symbol: DFNA5
  hgvsc: ENST00000419307.1:c.-281-4974A>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000473990
  gene symbol: DFNA5
  hgvsc: ENST00000473990.1:n.67A>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000386670
  ensembl transcript: ENST00000409775
  gene symbol: DFNA5
  hgvsc: ENST00000409775.3:c.47A>T
  hgvsp: ENSP00000386670.3:p.Asp16Val
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105928
  ensembl transcript: ENST00000493723
  gene symbol: DFNA5
  hgvsc: ENST00000493723.1:n.66A>T
  variant of: http://identifiers.org/hgnc/2810
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105928
  ensembl protein: ENSP00000413963
  ensembl transcript: ENST00000414428
  gene symbol: DFNA5
  hgvsc: ENST00000414428.1:c.-281-4974A>T
  variant of: http://identifiers.org/hgnc/2810
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15639
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp16Val
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10617
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4561
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3452
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9394
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66326
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.144081e6

QD
type: SiteQuality
SIO_000300: 1.244e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.785e0

VQSLOD
type: SiteQuality
SIO_000300: 1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 5.133e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.105e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4560
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25480
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66276
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.142479e6

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

QD
type: SiteQuality
SIO_000300: 1.452e1

MQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.109e0

FS
type: SiteQuality
SIO_000300: 1.179e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66266
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.141987e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.512e0

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 52
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

Latino
type: Population
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: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509661835748792e-5
allele num: 66240
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

FS
type: SiteQuality
SIO_000300: 3.256e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 1.294e1

DP
type: SiteQuality
SIO_000300: 2.141352e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.429999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66230
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 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: 6612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.048e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.87e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.140741e6

VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 3.082e1

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 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: 1
allele frequency: 1.511213201958532e-5
allele num: 66172
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.488e1

FS
type: SiteQuality
SIO_000300: 4.497e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.894e0

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.871e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 2.139113e6

GenotypeQuality
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bin: 2.75e1
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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bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.058201058201058e-4
allele num: 66150
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

FS
type: SiteQuality
SIO_000300: 1.173e0

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.57e-1

DP
type: SiteQuality
SIO_000300: 2.138529e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.087909411907951e-5
allele num: 16426
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

DP
type: SiteQuality
SIO_000300: 2.136472e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66034
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.097560975609756e-5
allele num: 16400
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QD
type: SiteQuality
SIO_000300: 1.184e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.130024e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.053e1

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

MQRankSum
type: SiteQuality
SIO_000300: 2.06e0

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
all individuals: 63
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GenotypeQuality
all individuals: 1356
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.489792357354738e-4
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65942
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

FS
type: SiteQuality
SIO_000300: 3.936e0

MQ
type: SiteQuality
SIO_000300: 6.044e1

QD
type: SiteQuality
SIO_000300: 2.204e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

DP
type: SiteQuality
SIO_000300: 2.121054e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.52e-2

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65936
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.617344268016053e-4
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

FS
type: SiteQuality
SIO_000300: 3.582e0

QD
type: SiteQuality
SIO_000300: 1.032e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.19e-1

DP
type: SiteQuality
SIO_000300: 2.120141e6

MQRankSum
type: SiteQuality
SIO_000300: -1.043e0

MQ
type: SiteQuality
SIO_000300: 6.029e1

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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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65886
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.41e-1

DP
type: SiteQuality
SIO_000300: 2.109903e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518003521768171e-5
allele num: 65876
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.071e0

VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

DP
type: SiteQuality
SIO_000300: 2.107869e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 3.853e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.042e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.14e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 134
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519387383007172e-5
allele num: 65816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.09623e6

VQSLOD
type: SiteQuality
SIO_000300: -9.579e-1

QD
type: SiteQuality
SIO_000300: 2.599e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.933999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.427e0

GenotypeQuality
all individuals: 3019
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 22757
bin: 6.25e1
variant carriers: 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: 10068
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65732
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.371e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 2.645e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.903e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

DP
type: SiteQuality
SIO_000300: 2.076942e6

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

MQ
type: SiteQuality
SIO_000300: 6.031e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1788
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.161424296097234e-5
allele num: 65492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
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: 892
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.516e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.03428e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.106e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-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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variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

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

East Asian
type: Population
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allele frequency: 1.165229550221394e-4
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
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QD
type: SiteQuality
SIO_000300: 1.036e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.75e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.913e1

DP
type: SiteQuality
SIO_000300: 2.033459e6

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

GenotypeQuality
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bin: 2.75e1
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: 6.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

South Asian
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allele frequency: 6.136475208640157e-5
allele num: 16296
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African
type: Population
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65420
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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FS
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.027169e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 893
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166588894073728e-4
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.057169061449098e-5
allele num: 65420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.962143853357243e-5
allele num: 10038
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.027169e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.058e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
all individuals: 1884
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2928
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10489
bin: 9.75e1
variant carriers: 44

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65390
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.989834562487542e-4
allele num: 10034
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

East Asian
type: Population
allele count: 43
allele frequency: 5.016332244517033e-3
allele num: 8572
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.019248e6

QD
type: SiteQuality
SIO_000300: 1.156e1

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 215
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16248
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1336
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10445
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534589650727396e-5
allele num: 65164
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.118e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.1e-3

QD
type: SiteQuality
SIO_000300: 1.481e1

DP
type: SiteQuality
SIO_000300: 1.977409e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

GenotypeQuality
all individuals: 5990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10447
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2398
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1774
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.143449546920596e-5
allele num: 65110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.714e0

VQSLOD
type: SiteQuality
SIO_000300: -2.279e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.41e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.175e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

DP
type: SiteQuality
SIO_000300: 1.965291e6

MQ
type: SiteQuality
SIO_000300: 6.056e1

GenotypeQuality
all individuals: 2864
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5680
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10449
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1705
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.548467017652524e-4
allele num: 6458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.079114509465376e-4
allele num: 64868
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: 8544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.546e1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.605e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.595e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.009e1

DP
type: SiteQuality
SIO_000300: 1.951927e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.77e-1

GenotypeQuality
all individuals: 956
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2125
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1004
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7502
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 207
allele frequency: 3.773240977032447e-2
allele num: 5486
num of homozygotes: 3

Other
type: Population
allele count: 1
allele frequency: 1.689189189189189e-3
allele num: 592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.271075581395349e-5
allele num: 44032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5550
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 4.012345679012346e-3
allele num: 3240
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.592541673827119e-5
allele num: 11638
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.961733e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.09e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

QD
type: SiteQuality
SIO_000300: 1.769e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

MQ
type: SiteQuality
SIO_000300: 5.757e1

GenotypeQuality
all individuals: 1807
bin: 8.25e1
variant carriers: 1671

GenotypeQuality
all individuals: 680
bin: 4.25e1
variant carriers: 395

GenotypeQuality
all individuals: 285
bin: 1.75e1
variant carriers: 190

GenotypeQuality
all individuals: 35218
bin: 9.75e1
variant carriers: 34232

GenotypeQuality
all individuals: 1381
bin: 3.25e1
variant carriers: 335

GenotypeQuality
all individuals: 871
bin: 5.75e1
variant carriers: 714

GenotypeQuality
all individuals: 1262
bin: 5.25e1
variant carriers: 1069

GenotypeQuality
all individuals: 844
bin: 2.75e1
variant carriers: 175

GenotypeQuality
all individuals: 2211
bin: 6.75e1
variant carriers: 1502

GenotypeQuality
all individuals: 1008
bin: 4.75e1
variant carriers: 792

GenotypeQuality
all individuals: 5754
bin: 6.25e1
variant carriers: 1411

GenotypeQuality
all individuals: 1064
bin: 7.25e1
variant carriers: 861

European (Non-Finnish)
type: Population
allele count: 30127
allele frequency: 4.686255599800896e-1
allele num: 64288
num of homozygotes: 7041

African
type: Population
allele count: 8385
allele frequency: 8.473120452708165e-1
allele num: 9896
num of homozygotes: 3536

European (Finnish)
type: Population
allele count: 3236
allele frequency: 5.007737542556484e-1
allele num: 6462
num of homozygotes: 790

South Asian
type: Population
allele count: 11671
allele frequency: 7.198100407055631e-1
allele num: 16214
num of homozygotes: 4207

East Asian
type: Population
allele count: 6787
allele frequency: 7.994110718492344e-1
allele num: 8490
num of homozygotes: 2709

Latino
type: Population
allele count: 8334
allele frequency: 7.393541518807665e-1
allele num: 11272
num of homozygotes: 3115

Other
type: Population
allele count: 502
allele frequency: 5.730593607305936e-1
allele num: 876
num of homozygotes: 139

QD
type: SiteQuality
SIO_000300: 2.331e1

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.180000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

FS
type: SiteQuality
SIO_000300: 7.84e-1

DP
type: SiteQuality
SIO_000300: 2.310295e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

GenotypeQuality
all individuals: 861
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4677
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12501
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 564
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5464
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4980
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.274898767004868e-5
allele num: 43958
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.946094e6

MQRankSum
type: SiteQuality
SIO_000300: 9.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.17e-2

FS
type: SiteQuality
SIO_000300: 1.766e0

MQ
type: SiteQuality
SIO_000300: 6.134e1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e-1

QD
type: SiteQuality
SIO_000300: 9.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 766
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 837
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 671
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 11956
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 911
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 436
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 536
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 766
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 6.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 64
allele frequency: 1.077078424772804e-2
allele num: 5942
num of homozygotes: 0

East Asian
type: Population
allele count: 102
allele frequency: 1.838500360490267e-2
allele num: 5548
num of homozygotes: 2

South Asian
type: Population
allele count: 23
allele frequency: 1.990652587848364e-3
allele num: 11554
num of homozygotes: 1

African
type: Population
allele count: 6
allele frequency: 1.2e-3
allele num: 5000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 513
allele frequency: 1.166598444535407e-2
allele num: 43974
num of homozygotes: 3

Latino
type: Population
allele count: 8
allele frequency: 2.444987775061125e-3
allele num: 3272
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.460207612456748e-3
allele num: 578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

DP
type: SiteQuality
SIO_000300: 1.944699e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.36e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.11e0

MQ
type: SiteQuality
SIO_000300: 6.006e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

QD
type: SiteQuality
SIO_000300: 1.596e1

GenotypeQuality
all individuals: 929
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4470
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7823
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4944
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6548
bin: 9.75e1
variant carriers: 14

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

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

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

East Asian
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allele frequency: 1.738698460009935e-3
allele num: 8052
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61980
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.340000000000001e-1

MQRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.8e-3

QD
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DP
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.03702128951924e-5
allele num: 65854
num of homozygotes: 0

Other
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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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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East Asian
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allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

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

Latino
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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: 896
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.055954527396632e-5
allele num: 65446
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.059e0

InbreedingCoeff
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SIO_000300: -1.1e-3

BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.439e1

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 1.253761283851555e-4
allele num: 7976
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 820
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South Asian
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allele frequency: 0.0e0
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FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
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SIO_000300: 1.022e1

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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.518833535844471e-4
allele num: 6584
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.782e0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.433e-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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

East Asian
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allele frequency: 1.179523472517103e-4
allele num: 8478
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
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allele frequency: 1.822821728034998e-4
allele num: 16458
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Other
type: Population
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
type: SiteQuality
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QD
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ClippingRankSum
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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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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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African
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South Asian
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Latino
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DP
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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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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East Asian
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Latino
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allele frequency: 3.565217391304348e-3
allele num: 11500
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European (Non-Finnish)
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allele frequency: 1.210727041588474e-4
allele num: 66076
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African
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allele frequency: 4.723707664884135e-2
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Other
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allele num: 900
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European (Finnish)
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South Asian
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VQSLOD
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QD
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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Other
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ClippingRankSum
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QD
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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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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African
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
type: Population
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allele num: 8508
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510391493475109e-5
allele num: 66208
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.15e0

VQSLOD
type: SiteQuality
SIO_000300: -1.422e0

QD
type: SiteQuality
SIO_000300: 1.512e1

MQ
type: SiteQuality
SIO_000300: 5.805e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.160359e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509251713000694e-5
allele num: 66258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

VQSLOD
type: SiteQuality
SIO_000300: -6.479e-1

FS
type: SiteQuality
SIO_000300: 2.916e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.826e1

MQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

DP
type: SiteQuality
SIO_000300: 2.161365e6

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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
all individuals: 22
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.53e1

VQSLOD
type: SiteQuality
SIO_000300: -1.942e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 1.1594e1

DP
type: SiteQuality
SIO_000300: 2.158093e6

MQRankSum
type: SiteQuality
SIO_000300: -1.125e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.351e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005168890491646e-5
allele num: 66552
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.158248e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

FS
type: SiteQuality
SIO_000300: 2.724e0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9343
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e0

DP
type: SiteQuality
SIO_000300: 2.158925e6

MQ
type: SiteQuality
SIO_000300: 5.84e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.089e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.487e0

QD
type: SiteQuality
SIO_000300: 1.169e1

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

FS
type: SiteQuality
SIO_000300: 7.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.269e0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9189
bin: 9.75e1
variant carriers: 3

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001560811622043e-5
allele num: 66632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

DP
type: SiteQuality
SIO_000300: 2.159935e6

FS
type: SiteQuality
SIO_000300: 5.808e0

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

VQSLOD
type: SiteQuality
SIO_000300: -4.802e-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
all individuals: 10
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e0

MQ
type: SiteQuality
SIO_000300: 5.862e1

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

East Asian
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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: 908
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.890173410404624e-4
allele num: 10380
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.883e1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
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
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

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

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: 8626
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.517e0

MQ
type: SiteQuality
SIO_000300: 5.758e1

DP
type: SiteQuality
SIO_000300: 2.161608e6

QD
type: SiteQuality
SIO_000300: 1.312e1

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9188
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998320940273447e-5
allele num: 66704
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.925298421255295e-4
allele num: 10388
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

FS
type: SiteQuality
SIO_000300: 1.149e0

DP
type: SiteQuality
SIO_000300: 2.161884e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.829e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 4228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9185
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.228e1

DP
type: SiteQuality
SIO_000300: 2.161547e6

FS
type: SiteQuality
SIO_000300: 1.767e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5193
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variant carriers: 0

GenotypeQuality
all individuals: 9360
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.192e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.168e0

MQRankSum
type: SiteQuality
SIO_000300: -4.51e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

FS
type: SiteQuality
SIO_000300: 6.447e0

QD
type: SiteQuality
SIO_000300: 1.06e1

VQSLOD
type: SiteQuality
SIO_000300: -2.077e0

DP
type: SiteQuality
SIO_000300: 2.161707e6

GenotypeQuality
all individuals: 5194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4228
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 4015
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.769e1

DP
type: SiteQuality
SIO_000300: 2.162328e6

MQRankSum
type: SiteQuality
SIO_000300: 3.21e0

VQSLOD
type: SiteQuality
SIO_000300: -2.354e0

FS
type: SiteQuality
SIO_000300: 6.288e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.593e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.325e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e0

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

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

GenotypeQuality
all individuals: 5193
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23870
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.961e0

DP
type: SiteQuality
SIO_000300: 2.162306e6

QD
type: SiteQuality
SIO_000300: 1.292e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-2

FS
type: SiteQuality
SIO_000300: 3.22e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

GenotypeQuality
all individuals: 5193
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23873
bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

QD
type: SiteQuality
SIO_000300: 1.915e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.289e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 2.162452e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 23884
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.944e1

DP
type: SiteQuality
SIO_000300: 2.162454e6

MQ
type: SiteQuality
SIO_000300: 5.937e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.958e0

MQRankSum
type: SiteQuality
SIO_000300: -1.893e0

VQSLOD
type: SiteQuality
SIO_000300: -2.453e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.09e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 9364
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.106e1

MQRankSum
type: SiteQuality
SIO_000300: -4.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.054e0

DP
type: SiteQuality
SIO_000300: 2.162513e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.86e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9187
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variant carriers: 6

GenotypeQuality
all individuals: 2117
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4227
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.990649724286742e-5
allele num: 66736
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 2.163333e6

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.316e1

GenotypeQuality
all individuals: 9366
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9181
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.644e1

MQRankSum
type: SiteQuality
SIO_000300: -1.19e0

FS
type: SiteQuality
SIO_000300: 1.757e0

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

MQ
type: SiteQuality
SIO_000300: 5.708e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.162757e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4227
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9181
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.26e-1

DP
type: SiteQuality
SIO_000300: 2.162777e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.372e1

MQ
type: SiteQuality
SIO_000300: 5.892e1

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.244e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e0

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

GenotypeQuality
all individuals: 2110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 137

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 137
allele frequency: 2.052865020378806e-3
allele num: 66736
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

QD
type: SiteQuality
SIO_000300: 1.204e1

FS
type: SiteQuality
SIO_000300: 5.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 2.181478e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

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

GenotypeQuality
all individuals: 9352
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4003
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variant carriers: 0

GenotypeQuality
all individuals: 5182
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

FS
type: SiteQuality
SIO_000300: 5.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

QD
type: SiteQuality
SIO_000300: 1.204e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

DP
type: SiteQuality
SIO_000300: 2.181478e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.204e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

FS
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 2.181478e6

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

GenotypeQuality
all individuals: 4007
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2695
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.923e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.004e1

FS
type: SiteQuality
SIO_000300: 1.938e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.29e-1

DP
type: SiteQuality
SIO_000300: 2.162301e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4007
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 4.801e0

QD
type: SiteQuality
SIO_000300: 2.62e0

MQ
type: SiteQuality
SIO_000300: 5.094e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.396e0

MQRankSum
type: SiteQuality
SIO_000300: -8.154e0

DP
type: SiteQuality
SIO_000300: 2.162216e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.77e0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4009
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.295e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.904e0

MQRankSum
type: SiteQuality
SIO_000300: -1.893e0

DP
type: SiteQuality
SIO_000300: 2.162557e6

FS
type: SiteQuality
SIO_000300: 1.752e0

VQSLOD
type: SiteQuality
SIO_000300: -1.506e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
all individuals: 5175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9249
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

QD
type: SiteQuality
SIO_000300: 1.313e1

DP
type: SiteQuality
SIO_000300: 2.188246e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.84e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 8.75e1
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GenotypeQuality
all individuals: 9249
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variant carriers: 180

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 5175
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variant carriers: 0

GenotypeQuality
all individuals: 4224
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 23895
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

South Asian
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allele count: 171
allele frequency: 1.035735917625681e-2
allele num: 16510
num of homozygotes: 2

African
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allele count: 5
allele frequency: 4.805843906189927e-4
allele num: 10404
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.313e1

FS
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.84e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

MQ
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SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-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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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 4.958e0

QD
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DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
type: SiteQuality
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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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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16510
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
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African
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allele count: 0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 4.958e0

InbreedingCoeff
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MQ
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SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

BaseQRankSum
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SIO_000300: 1.47e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.161317e6

QD
type: SiteQuality
SIO_000300: 1.328e1

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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.990649724286742e-5
allele num: 66736
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.216e1

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 5.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.133e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 2.161605e6

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele 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: 1.498576352465158e-5
allele num: 66730
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.429e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.3e-2

FS
type: SiteQuality
SIO_000300: 1.386e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.121e-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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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
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Latino
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allele frequency: 0.0e0
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South Asian
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East Asian
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African
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allele frequency: 9.613535858488752e-5
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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QD
type: SiteQuality
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
type: SiteQuality
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