4-2929932-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929932
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929932
    reference: chr 4
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1896T>C
  hgvsp: ENST00000398129.1:c.1896T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1710T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.402T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.239T>C
  hgvsp: ENSP00000438069.1:p.Val80Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.1989T>C
  hgvsp: ENST00000264758.7:c.1989T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.265T>C
  hgvsp: ENSP00000441388.1:p.Val89Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*34T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1896T>C
  hgvsp: ENST00000446856.1:c.1896T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*34T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*34T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1106T>C
  hgvsp: ENST00000514940.1:c.1106T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*34T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*34T>C
  variant of: http://identifiers.org/hgnc/243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val80Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

4-2929940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929940
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929940
    reference: chr 4
allele count: 6
allele frequency: 4.942583653228331e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.247C>T
  hgvsp: ENSP00000438069.1:p.Pro83Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.410C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*42C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1904C>T
  hgvsp: ENSP00000381197.1:p.Ala635Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1904C>T
  hgvsp: ENSP00000399828.1:p.Ala635Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.273C>T
  hgvsp: ENSP00000441388.1:p.Pro92Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.1997C>T
  hgvsp: ENSP00000264758.6:p.Ala666Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1114C>T
  hgvsp: ENSP00000424143.1:p.Ala372Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*42C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10249
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala666Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

4-2929942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929942
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929942
    reference: chr 4
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*44A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*44A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1116A>G
  hgvsp: ENSP00000424143.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.1999A>G
  hgvsp: ENSP00000264758.6:p.Thr667Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.275A>G
  hgvsp: ENST00000541843.1:c.275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1906A>G
  hgvsp: ENSP00000381197.1:p.Thr636Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*44A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.412A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*44A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*44A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1720A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1906A>G
  hgvsp: ENSP00000399828.1:p.Thr636Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.249A>G
  hgvsp: ENST00000536424.1:c.249A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr667Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

4-2929944-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929944
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929944
    reference: chr 4
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1908C>T
  hgvsp: ENST00000398129.1:c.1908C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1722C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1118C>T
  hgvsp: ENST00000514940.1:c.1118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.251C>T
  hgvsp: ENSP00000438069.1:p.Pro84Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.414C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1908C>T
  hgvsp: ENST00000446856.1:c.1908C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*46C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*46C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*46C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.277C>T
  hgvsp: ENSP00000441388.1:p.Pro93Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*46C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*46C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2001C>T
  hgvsp: ENST00000264758.7:c.2001C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro84Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

4-2929954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929954
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929954
    reference: chr 4
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.261A>G
  hgvsp: ENST00000536424.1:c.261A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*56A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*56A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*56A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1918A>G
  hgvsp: ENSP00000399828.1:p.Thr640Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.287A>G
  hgvsp: ENST00000541843.1:c.287A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1918A>G
  hgvsp: ENSP00000381197.1:p.Thr640Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1128A>G
  hgvsp: ENSP00000424143.1:p.Thr377Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*56A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2011A>G
  hgvsp: ENSP00000264758.6:p.Thr671Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.424A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*56A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1732A>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr671Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/4-2929955-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929955
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929955
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.262C>A
  hgvsp: ENSP00000438069.1:p.Leu88Ile
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.288C>A
  hgvsp: ENSP00000441388.1:p.Leu97Ile
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1733C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*57C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.425C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1919C>A
  hgvsp: ENSP00000381197.1:p.Thr640Asn
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*57C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*57C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2012C>A
  hgvsp: ENSP00000264758.6:p.Thr671Asn
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*57C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1919C>A
  hgvsp: ENSP00000399828.1:p.Thr640Asn
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1129C>A
  hgvsp: ENSP00000424143.1:p.Thr377Asn
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*57C>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr671Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-2929962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929962
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929962
    reference: chr 4
allele count: 8
allele frequency: 6.589568712727751e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.295C>T
  hgvsp: ENSP00000441388.1:p.Pro99Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1136C>T
  hgvsp: ENST00000514940.1:c.1136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2019C>T
  hgvsp: ENST00000264758.7:c.2019C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*64C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*64C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.432C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.269C>T
  hgvsp: ENSP00000438069.1:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*64C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1926C>T
  hgvsp: ENST00000398129.1:c.1926C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1926C>T
  hgvsp: ENST00000446856.1:c.1926C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1740C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*64C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*64C>T
  variant of: http://identifiers.org/hgnc/243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro90Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

4-2929963-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929963
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929963
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1927G>C
  hgvsp: ENSP00000381197.1:p.Asp643His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2020G>C
  hgvsp: ENSP00000264758.6:p.Asp674His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*65G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1927G>C
  hgvsp: ENSP00000399828.1:p.Asp643His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.296G>C
  hgvsp: ENST00000541843.1:c.296G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1137G>C
  hgvsp: ENSP00000424143.1:p.Asp380His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*65G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1741G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*65G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.270G>C
  hgvsp: ENST00000536424.1:c.270G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.433G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*65G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*65G>C
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp674His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

4-2929964-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929964
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929964
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*66A>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.297A>T
  hgvsp: ENSP00000441388.1:p.Ile100Phe
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1928A>T
  hgvsp: ENSP00000399828.1:p.Asp643Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1138A>T
  hgvsp: ENSP00000424143.1:p.Asp380Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.271A>T
  hgvsp: ENSP00000438069.1:p.Ile91Phe
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2021A>T
  hgvsp: ENSP00000264758.6:p.Asp674Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*66A>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1928A>T
  hgvsp: ENSP00000381197.1:p.Asp643Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1742A>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.434A>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*66A>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*66A>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*66A>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp674Val
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

4-2929964-ATCTGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929964
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929959
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1929_1933delTCTGT
  hgvsp: ENSP00000399828.1:p.Leu644ProfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.272_276delTCTGT
  hgvsp: ENSP00000438069.1:p.Ile91ThrfsTer94
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1929_1933delTCTGT
  hgvsp: ENSP00000381197.1:p.Leu644ProfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.298_302delTCTGT
  hgvsp: ENSP00000441388.1:p.Ile100ThrfsTer?
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2022_2026delTCTGT
  hgvsp: ENSP00000264758.6:p.Leu675ProfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.435_439delTCTGT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*67_*71delTCTGT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*67_*71delTCTGT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*67_*71delTCTGT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1139_1143delTCTGT
  hgvsp: ENSP00000424143.1:p.Leu381ProfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1743_1747delTCTGT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*67_*71delTCTGT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*67_*71delTCTGT
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu675ProfsTer2
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: ATCTGT
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-2929966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929966
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929966
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*68C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1930C>T
  hgvsp: ENST00000446856.1:c.1930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.299C>T
  hgvsp: ENST00000541843.1:c.299C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1140C>T
  hgvsp: ENST00000514940.1:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1744C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.436C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1930C>T
  hgvsp: ENST00000398129.1:c.1930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*68C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2023C>T
  hgvsp: ENST00000264758.7:c.2023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*68C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*68C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.273C>T
  hgvsp: ENST00000536424.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*68C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu675Leu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-2929971-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929971
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929971
    reference: chr 4
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*73C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*73C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.304C>A
  hgvsp: ENSP00000441388.1:p.Pro102His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1935C>A
  hgvsp: ENST00000446856.1:c.1935C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.278C>A
  hgvsp: ENSP00000438069.1:p.Pro93His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1749C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*73C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2028C>A
  hgvsp: ENST00000264758.7:c.2028C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*73C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1935C>A
  hgvsp: ENST00000398129.1:c.1935C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1145C>A
  hgvsp: ENST00000514940.1:c.1145C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.441C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*73C>A
  variant of: http://identifiers.org/hgnc/243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro102His
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

4-2929971-CCCTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929971
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929967
    reference: chr 4
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.442_445delCCTG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*74_*77delCCTG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1146_1149delCCTG
  hgvsp: ENSP00000424143.1:p.Pro383MetfsTer12
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2029_2032delCCTG
  hgvsp: ENSP00000264758.6:p.Pro677MetfsTer12
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*74_*77delCCTG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*74_*77delCCTG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.279_282delCCTG
  hgvsp: ENSP00000438069.1:p.Leu94Ter
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1936_1939delCCTG
  hgvsp: ENSP00000381197.1:p.Pro646MetfsTer12
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.305_308delCCTG
  hgvsp: ENSP00000441388.1:p.Leu103Ter
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*74_*77delCCTG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1936_1939delCCTG
  hgvsp: ENSP00000399828.1:p.Pro646MetfsTer12
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1750_1753delCCTG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*74_*77delCCTG
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro677MetfsTer12
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: CCCTG
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

4-2929972-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929972
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929970
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.443_444delCT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1937_1938delCT
  hgvsp: ENSP00000381197.1:p.Pro646ArgfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*75_*76delCT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*75_*76delCT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1751_1752delCT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*75_*76delCT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1147_1148delCT
  hgvsp: ENSP00000424143.1:p.Pro383ArgfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*75_*76delCT
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.306_307delCT
  hgvsp: ENSP00000441388.1:p.Leu103AspfsTer?
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2030_2031delCT
  hgvsp: ENSP00000264758.6:p.Pro677ArgfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.280_281delCT
  hgvsp: ENSP00000438069.1:p.Leu94AspfsTer92
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1937_1938delCT
  hgvsp: ENSP00000399828.1:p.Pro646ArgfsTer2
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*75_*76delCT
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro677ArgfsTer2
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CCT
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/4-2929976-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929976
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929976
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1754A>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*78A>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.283A>C
  hgvsp: ENSP00000438069.1:p.Met95Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.446A>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*78A>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1940A>C
  hgvsp: ENSP00000399828.1:p.Asp647Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*78A>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1940A>C
  hgvsp: ENSP00000381197.1:p.Asp647Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2033A>C
  hgvsp: ENSP00000264758.6:p.Asp678Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1150A>C
  hgvsp: ENSP00000424143.1:p.Asp384Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.309A>C
  hgvsp: ENSP00000441388.1:p.Met104Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*78A>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*78A>C
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp678Ala
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

4-2929976-ATGAACCTTCAGAAGCACTCGGCTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929976
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929952
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsp: ENSP00000381197.1:p.Glu648_Phe655del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsp: ENSP00000424143.1:p.Glu385_Phe392del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsp: ENSP00000264758.6:p.Glu679_Phe686del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsp: ENSP00000399828.1:p.Glu648_Phe655del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu679_Phe686del
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: ATGAACCTTCAGAAGCACTCGGCTT
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

4-2929977-TGAACCTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929977
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929969
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.285_292delGAACCTTC
  hgvsp: ENSP00000438069.1:p.Met95IlefsTer89
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*80_*87delGAACCTTC
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*80_*87delGAACCTTC
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsp: ENSP00000424143.1:p.Glu385ArgfsTer16
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsp: ENSP00000399828.1:p.Glu648ArgfsTer16
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsp: ENSP00000264758.6:p.Glu679ArgfsTer16
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsp: ENSP00000381197.1:p.Glu648ArgfsTer16
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*80_*87delGAACCTTC
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.448_455delGAACCTTC
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*80_*87delGAACCTTC
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.311_318delGAACCTTC
  hgvsp: ENSP00000441388.1:p.Met104IlefsTer?
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*80_*87delGAACCTTC
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu679ArgfsTer16
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: TGAACCTTC
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

4-2929981-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929981
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929981
    reference: chr 4
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1945C>G
  hgvsp: ENSP00000381197.1:p.Pro649Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.314C>G
  hgvsp: ENSP00000441388.1:p.Asn105Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.288C>G
  hgvsp: ENSP00000438069.1:p.Asn96Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*83C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1155C>G
  hgvsp: ENSP00000424143.1:p.Pro386Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1759C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*83C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*83C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1945C>G
  hgvsp: ENSP00000399828.1:p.Pro649Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*83C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.451C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*83C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2038C>G
  hgvsp: ENSP00000264758.6:p.Pro680Ala
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro680Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-2929982-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929982
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929982
    reference: chr 4
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.452C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2039C>A
  hgvsp: ENSP00000264758.6:p.Pro680His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.289C>A
  hgvsp: ENSP00000438069.1:p.Leu97Ile
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*84C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1946C>A
  hgvsp: ENSP00000381197.1:p.Pro649His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*84C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*84C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*84C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1946C>A
  hgvsp: ENSP00000399828.1:p.Pro649His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.315C>A
  hgvsp: ENSP00000441388.1:p.Leu106Ile
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1156C>A
  hgvsp: ENSP00000424143.1:p.Pro386His
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*84C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1760C>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro680His
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

4-2929988-AAGCACTCGGCTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929988
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929976
    reference: chr 4
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu682_Phe686delinsAsp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: AAGCACTCGGCTT
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

4-2929990-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929990
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929990
    reference: chr 4
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*92G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1954G>A
  hgvsp: ENSP00000381197.1:p.Ala652Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.323G>A
  hgvsp: ENST00000541843.1:c.323G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.297G>A
  hgvsp: ENST00000536424.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1164G>A
  hgvsp: ENSP00000424143.1:p.Ala389Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*92G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*92G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2047G>A
  hgvsp: ENSP00000264758.6:p.Ala683Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1768G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*92G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.460G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1954G>A
  hgvsp: ENSP00000399828.1:p.Ala652Thr
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala683Thr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

4-2929993-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929993
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929993
    reference: chr 4
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*95C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*95C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1167C>G
  hgvsp: ENSP00000424143.1:p.Leu390Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2050C>G
  hgvsp: ENSP00000264758.6:p.Leu684Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1771C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*95C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*95C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1957C>G
  hgvsp: ENSP00000381197.1:p.Leu653Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.300C>G
  hgvsp: ENSP00000438069.1:p.His100Gln
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*95C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1957C>G
  hgvsp: ENSP00000399828.1:p.Leu653Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.326C>G
  hgvsp: ENSP00000441388.1:p.His109Gln
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.463C>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu684Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

4-2929993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929993
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929993
    reference: chr 4
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1771C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1957C>T
  hgvsp: ENSP00000381197.1:p.Leu653Phe
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*95C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*95C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2050C>T
  hgvsp: ENSP00000264758.6:p.Leu684Phe
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*95C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.300C>T
  hgvsp: ENST00000536424.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1167C>T
  hgvsp: ENSP00000424143.1:p.Leu390Phe
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*95C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1957C>T
  hgvsp: ENSP00000399828.1:p.Leu653Phe
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*95C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.326C>T
  hgvsp: ENST00000541843.1:c.326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.463C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu684Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

4-2929995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929995
    reference: chr 4
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*97C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1959C>T
  hgvsp: ENST00000398129.1:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*97C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*97C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.328C>T
  hgvsp: ENSP00000441388.1:p.Ser110Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1959C>T
  hgvsp: ENST00000446856.1:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.465C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2052C>T
  hgvsp: ENST00000264758.7:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1773C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1169C>T
  hgvsp: ENST00000514940.1:c.1169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.302C>T
  hgvsp: ENSP00000438069.1:p.Ser101Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*97C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*97C>T
  variant of: http://identifiers.org/hgnc/243
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser101Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

4-2929996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929996
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929996
    reference: chr 4
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2053G>A
  hgvsp: ENSP00000264758.6:p.Gly685Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1774G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.303G>A
  hgvsp: ENST00000536424.1:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*98G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.329G>A
  hgvsp: ENST00000541843.1:c.329G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.466G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1960G>A
  hgvsp: ENSP00000381197.1:p.Gly654Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1170G>A
  hgvsp: ENSP00000424143.1:p.Gly391Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*98G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*98G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1960G>A
  hgvsp: ENSP00000399828.1:p.Gly654Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*98G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*98G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly685Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-2929996-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2929996
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929996
    reference: chr 4
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.329G>C
  hgvsp: ENST00000541843.1:c.329G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1960G>C
  hgvsp: ENSP00000381197.1:p.Gly654Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2053G>C
  hgvsp: ENSP00000264758.6:p.Gly685Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*98G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*98G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.303G>C
  hgvsp: ENST00000536424.1:c.303G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1170G>C
  hgvsp: ENSP00000424143.1:p.Gly391Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*98G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*98G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.466G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*98G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1960G>C
  hgvsp: ENSP00000399828.1:p.Gly654Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1774G>C
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly685Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

4-2930002-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930002
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930002
    reference: chr 4
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.472C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1966C>T
  hgvsp: ENSP00000399828.1:p.Pro656Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*104C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.335C>T
  hgvsp: ENST00000541843.1:c.335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1966C>T
  hgvsp: ENSP00000381197.1:p.Pro656Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*104C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1780C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1176C>T
  hgvsp: ENSP00000424143.1:p.Pro393Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2059C>T
  hgvsp: ENSP00000264758.6:p.Pro687Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*104C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*104C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.309C>T
  hgvsp: ENST00000536424.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*104C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro687Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

4-2930002-CCAATGTTAGAGAAGGAGGAGGAAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930002
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2929978
    reference: chr 4
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsp: ENSP00000381197.1:p.Met657_Ala664del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsp: ENSP00000424143.1:p.Met394_Ala401del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsp: ENSP00000399828.1:p.Met657_Ala664del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsp: ENSP00000264758.6:p.Met688_Ala695del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met688_Ala695del
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: CCAATGTTAGAGAAGGAGGAGGAAG
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-2930006-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930006
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930006
    reference: chr 4
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*108T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*108T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1970T>C
  hgvsp: ENSP00000381197.1:p.Met657Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1970T>C
  hgvsp: ENSP00000399828.1:p.Met657Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1180T>C
  hgvsp: ENSP00000424143.1:p.Met394Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.339T>C
  hgvsp: ENSP00000441388.1:p.Cys114Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.313T>C
  hgvsp: ENSP00000438069.1:p.Cys105Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*108T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2063T>C
  hgvsp: ENSP00000264758.6:p.Met688Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.476T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*108T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1784T>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*108T>C
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met688Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-2930014-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930014
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930014
    reference: chr 4
allele count: 145
allele frequency: 1.195442478605702e-3
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*116A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*3A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1978A>G
  hgvsp: ENSP00000381197.1:p.Lys660Glu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*116A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*116A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1188A>G
  hgvsp: ENSP00000424143.1:p.Lys397Glu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2071A>G
  hgvsp: ENSP00000264758.6:p.Lys691Glu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1978A>G
  hgvsp: ENSP00000399828.1:p.Lys660Glu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*116A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*3A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1792A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*116A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.484A>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10208
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.75e1
  variant carriers: 127
genotype quality: GenotypeQuality
hgvs: p.Lys691Glu
num of homozygotes: 4
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

4-2930017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930017
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930017
    reference: chr 4
allele count: 20
allele frequency: 1.648858989579211e-4
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*119G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*6G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*119G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000503062
  gene symbol: ADD1
  hgvsc: ENST00000503062.1:n.487G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1981G>A
  hgvsp: ENSP00000399828.1:p.Glu661Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*6G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*119G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2074G>A
  hgvsp: ENSP00000264758.6:p.Glu692Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*119G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1191G>A
  hgvsp: ENSP00000424143.1:p.Glu398Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1981G>A
  hgvsp: ENSP00000381197.1:p.Glu661Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*119G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1795G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu692Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

4-2930020-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930020
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930020
    reference: chr 4
allele count: 7
allele frequency: 5.772814989526464e-5
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1798G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1984G>A
  hgvsp: ENSP00000399828.1:p.Glu662Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*122G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2077G>A
  hgvsp: ENSP00000264758.6:p.Glu693Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*122G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1194G>A
  hgvsp: ENSP00000424143.1:p.Glu399Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1984G>A
  hgvsp: ENSP00000381197.1:p.Glu662Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*122G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*122G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*122G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu693Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

4-2930026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930026
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930026
    reference: chr 4
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1200G>A
  hgvsp: ENSP00000424143.1:p.Ala401Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1990G>A
  hgvsp: ENSP00000381197.1:p.Ala664Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1990G>A
  hgvsp: ENSP00000399828.1:p.Ala664Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2083G>A
  hgvsp: ENSP00000264758.6:p.Ala695Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*128G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*128G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*128G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1804G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*128G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*128G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala695Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

4-2930030-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930030
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930030
    reference: chr 4
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1204A>G
  hgvsp: ENSP00000424143.1:p.His402Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*19A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1994A>G
  hgvsp: ENSP00000399828.1:p.His665Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1994A>G
  hgvsp: ENSP00000381197.1:p.His665Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2087A>G
  hgvsp: ENSP00000264758.6:p.His696Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*132A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*132A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*132A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*132A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*132A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*19A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1808A>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His696Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-2930035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930035
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930035
    reference: chr 4
allele count: 5
allele frequency: 4.129569368506252e-5
allele num: 121078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*137C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.1999C>T
  hgvsp: ENSP00000399828.1:p.Pro667Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1813C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1209C>T
  hgvsp: ENSP00000424143.1:p.Pro404Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*137C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2092C>T
  hgvsp: ENSP00000264758.6:p.Pro698Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.1999C>T
  hgvsp: ENSP00000381197.1:p.Pro667Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*137C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*24C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*137C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*137C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*24C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro698Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

4-2930036-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930036
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930036
    reference: chr 4
allele count: 51
allele frequency: 4.212717450562522e-4
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*138C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1814C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*25C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1210C>G
  hgvsp: ENSP00000424143.1:p.Pro404Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2000C>G
  hgvsp: ENSP00000399828.1:p.Pro667Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*138C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2093C>G
  hgvsp: ENSP00000264758.6:p.Pro698Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*138C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2000C>G
  hgvsp: ENSP00000381197.1:p.Pro667Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*138C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*138C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*25C>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12158
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10080
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro698Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-2930041-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930041
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930041
    reference: chr 4
allele count: 2
allele frequency: 1.653247805313538e-5
allele num: 120974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*143A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*143A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2005A>G
  hgvsp: ENSP00000399828.1:p.Ser669Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*143A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2005A>G
  hgvsp: ENSP00000381197.1:p.Ser669Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1215A>G
  hgvsp: ENSP00000424143.1:p.Ser406Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*143A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2098A>G
  hgvsp: ENSP00000264758.6:p.Ser700Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1819A>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*143A>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser700Gly
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/4-2930044-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930044
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930044
    reference: chr 4
allele count: 3
allele frequency: 2.481800132362674e-5
allele num: 120880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*146C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*146C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1822C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*33C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*146C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2008C>A
  hgvsp: ENSP00000381197.1:p.Pro670Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2101C>A
  hgvsp: ENSP00000264758.6:p.Pro701Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*146C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2008C>A
  hgvsp: ENSP00000399828.1:p.Pro670Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1218C>A
  hgvsp: ENSP00000424143.1:p.Pro407Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*33C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*146C>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro701Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

4-2930053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930053
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930053
    reference: chr 4
allele count: 2
allele frequency: 1.657605092162843e-5
allele num: 120656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*155G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1227G>A
  hgvsp: ENSP00000424143.1:p.Ala410Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2017G>A
  hgvsp: ENSP00000399828.1:p.Ala673Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*155G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2017G>A
  hgvsp: ENSP00000381197.1:p.Ala673Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*155G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2110G>A
  hgvsp: ENSP00000264758.6:p.Ala704Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1831G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*155G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*155G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala704Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

4-2930053-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930053
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930053
    reference: chr 4
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*155G>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*155G>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2017G>T
  hgvsp: ENSP00000381197.1:p.Ala673Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*155G>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1831G>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*42G>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1227G>T
  hgvsp: ENSP00000424143.1:p.Ala410Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2110G>T
  hgvsp: ENSP00000264758.6:p.Ala704Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*155G>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2017G>T
  hgvsp: ENSP00000399828.1:p.Ala673Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*155G>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*42G>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala704Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

4-2930065-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930065
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930065
    reference: chr 4
allele count: 1
allele frequency: 8.352404657300837e-6
allele num: 119726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2029G>C
  hgvsp: ENSP00000381197.1:p.Ala677Pro
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2029G>C
  hgvsp: ENSP00000399828.1:p.Ala677Pro
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2122G>C
  hgvsp: ENSP00000264758.6:p.Ala708Pro
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*54G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*167G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*54G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1843G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*167G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1239G>C
  hgvsp: ENSP00000424143.1:p.Ala414Pro
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*167G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*167G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*167G>C
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9461
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala708Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/4-2930070-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930070
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930070
    reference: chr 4
allele count: 1
allele frequency: 8.357430591538938e-6
allele num: 119654
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2127C>A
  hgvsp: ENSP00000264758.6:p.Ser709Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*172C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*172C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1244C>A
  hgvsp: ENSP00000424143.1:p.Ser415Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*59C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2034C>A
  hgvsp: ENSP00000381197.1:p.Ser678Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*172C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*172C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2034C>A
  hgvsp: ENSP00000399828.1:p.Ser678Arg
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*59C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1848C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*172C>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser709Arg
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-2930073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930073
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930073
    reference: chr 4
allele count: 4
allele frequency: 3.351992759695639e-5
allele num: 119332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1247C>T
  hgvsp: ENST00000514940.1:c.1247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*175C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000441388
  ensembl transcript: ENST00000541843
  gene symbol: ADD1
  hgvsc: ENST00000541843.1:c.*62C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2037C>T
  hgvsp: ENST00000446856.1:c.2037C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*62C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*175C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*175C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1851C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*175C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2130C>T
  hgvsp: ENST00000264758.7:c.2130C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2037C>T
  hgvsp: ENST00000398129.1:c.2037C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*175C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro710Pro
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-2930074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930074
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930074
    reference: chr 4
allele count: 5
allele frequency: 4.187534547160014e-5
allele num: 119402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2131G>A
  hgvsp: ENSP00000264758.6:p.Glu711Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*63G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*176G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*176G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2038G>A
  hgvsp: ENSP00000381197.1:p.Glu680Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1248G>A
  hgvsp: ENSP00000424143.1:p.Glu417Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2038G>A
  hgvsp: ENSP00000399828.1:p.Glu680Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*176G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*176G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1852G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9544
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu711Lys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

4-2930076-G-GCCAGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930076
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930082
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 119372
alternate allele: GCCAGCC
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2138_2143dupCCCCAG
  hgvsp: ENSP00000264758.6:p.Ala713_Pro714dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*183_*188dupCCCCAG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*183_*188dupCCCCAG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2045_2050dupCCCCAG
  hgvsp: ENSP00000381197.1:p.Ala682_Pro683dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*183_*188dupCCCCAG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*183_*188dupCCCCAG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2045_2050dupCCCCAG
  hgvsp: ENSP00000399828.1:p.Ala682_Pro683dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*183_*188dupCCCCAG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1859_1864dupCCCCAG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1255_1260dupCCCCAG
  hgvsp: ENSP00000424143.1:p.Ala419_Pro420dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*70_*75dupCCCCAG
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: inframe insertion
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala713_Pro714dup
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

4-2930076-GCCAGCCCCAGAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930076
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930064
    reference: chr 4
allele count: 1
allele frequency: 8.377173876620983e-6
allele num: 119372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsp: ENSP00000264758.6:p.Asp715_Pro718del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsp: ENSP00000381197.1:p.Asp684_Pro687del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsp: ENSP00000424143.1:p.Asp421_Pro424del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsp: ENSP00000399828.1:p.Asp684_Pro687del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3949
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp715_Pro718del
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: GCCAGCCCCAGAC
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-2930081-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930081
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930081
    reference: chr 4
allele count: 4
allele frequency: 3.352723249459373e-5
allele num: 119306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*70C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*183C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*183C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2138C>A
  hgvsp: ENSP00000264758.6:p.Ala713Asp
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1859C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2045C>A
  hgvsp: ENSP00000399828.1:p.Ala682Asp
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2045C>A
  hgvsp: ENSP00000381197.1:p.Ala682Asp
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*183C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1255C>A
  hgvsp: ENSP00000424143.1:p.Ala419Asp
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*183C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*183C>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala713Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

4-2930093-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930093
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930093
    reference: chr 4
allele count: 1
allele frequency: 8.399973120086016e-6
allele num: 119048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*195C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2057C>T
  hgvsp: ENSP00000399828.1:p.Ala686Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2057C>T
  hgvsp: ENSP00000381197.1:p.Ala686Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*195C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*195C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1871C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1267C>T
  hgvsp: ENSP00000424143.1:p.Ala423Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*82C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*195C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2150C>T
  hgvsp: ENSP00000264758.6:p.Ala717Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*195C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala717Val
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

4-2930095-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930095
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930095
    reference: chr 4
allele count: 4
allele frequency: 3.360723227638588e-5
allele num: 119022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*84C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1269C>G
  hgvsp: ENSP00000424143.1:p.Pro424Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*197C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2059C>G
  hgvsp: ENSP00000381197.1:p.Pro687Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*197C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2059C>G
  hgvsp: ENSP00000399828.1:p.Pro687Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*197C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*197C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2152C>G
  hgvsp: ENSP00000264758.6:p.Pro718Ala
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*197C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1873C>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9414
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro718Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

4-2930096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930096
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930096
    reference: chr 4
allele count: 1
allele frequency: 8.404773911581778e-6
allele num: 118980
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*198C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1874C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*198C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2060C>T
  hgvsp: ENSP00000399828.1:p.Pro687Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*198C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*198C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1270C>T
  hgvsp: ENSP00000424143.1:p.Pro424Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2060C>T
  hgvsp: ENSP00000381197.1:p.Pro687Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2153C>T
  hgvsp: ENSP00000264758.6:p.Pro718Leu
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*198C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro718Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-2930097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930097
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930097
    reference: chr 4
allele count: 2
allele frequency: 1.681322191771609e-5
allele num: 118954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*199G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*199G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*199G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1271G>A
  hgvsp: ENST00000514940.1:c.1271G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*199G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2061G>A
  hgvsp: ENST00000398129.1:c.2061G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*86G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2154G>A
  hgvsp: ENST00000264758.7:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2061G>A
  hgvsp: ENST00000446856.1:c.2061G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*199G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1875G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro718Pro
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

4-2930111-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930111
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930111
    reference: chr 4
allele count: 1
allele frequency: 8.415524960447032e-6
allele num: 118828
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2168C>G
  hgvsp: ENSP00000264758.6:p.Ala723Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*213C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2075C>G
  hgvsp: ENSP00000399828.1:p.Ala692Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*213C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1889C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*213C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*213C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*213C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1285C>G
  hgvsp: ENSP00000424143.1:p.Ala429Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2075C>G
  hgvsp: ENSP00000381197.1:p.Ala692Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*100C>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala723Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-2930114-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930114
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930114
    reference: chr 4
allele count: 16
allele frequency: 1.349846454965748e-4
allele num: 118532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*216C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*216C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*216C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2078C>G
  hgvsp: ENSP00000399828.1:p.Ala693Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1892C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2078C>G
  hgvsp: ENSP00000381197.1:p.Ala693Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*216C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1288C>G
  hgvsp: ENSP00000424143.1:p.Ala430Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2171C>G
  hgvsp: ENSP00000264758.6:p.Ala724Gly
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*103C>G
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*216C>G
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9068
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Ala724Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-2930115-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930115
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930115
    reference: chr 4
allele count: 1
allele frequency: 8.415666604951778e-6
allele num: 118826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1289C>A
  hgvsp: ENST00000514940.1:c.1289C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2079C>A
  hgvsp: ENST00000446856.1:c.2079C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*217C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2172C>A
  hgvsp: ENST00000264758.7:c.2172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2079C>A
  hgvsp: ENST00000398129.1:c.2079C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*217C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*217C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*217C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*217C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*104C>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1893C>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala724Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

4-2930116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930116
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930116
    reference: chr 4
allele count: 1
allele frequency: 8.414391976035812e-6
allele num: 118844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*218C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*218C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*218C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1894C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2080C>T
  hgvsp: ENSP00000381197.1:p.Pro694Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1290C>T
  hgvsp: ENSP00000424143.1:p.Pro431Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*105C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2173C>T
  hgvsp: ENSP00000264758.6:p.Pro725Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*218C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2080C>T
  hgvsp: ENSP00000399828.1:p.Pro694Ser
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*218C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro725Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-2930118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930118
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930118
    reference: chr 4
allele count: 1
allele frequency: 8.414958430105355e-6
allele num: 118836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*220C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*107C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1292C>T
  hgvsp: ENST00000514940.1:c.1292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2175C>T
  hgvsp: ENST00000264758.7:c.2175C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*220C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*220C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2082C>T
  hgvsp: ENST00000398129.1:c.2082C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*220C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2082C>T
  hgvsp: ENST00000446856.1:c.2082C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*220C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1896C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro725Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

4-2930124-T-TGTCGAGGAGGGGGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930124
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930139
    reference: chr 4
allele count: 1
allele frequency: 8.415949908266146e-6
allele num: 118822
alternate allele: TGTCGAGGAGGGGGCC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsp: ENSP00000264758.6:p.Val728_Ala732dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsp: ENSP00000381197.1:p.Val697_Ala701dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsp: ENSP00000399828.1:p.Val697_Ala701dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsp: ENSP00000424143.1:p.Val434_Ala438dup
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val728_Ala732dup
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

4-2930127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930127
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930127
    reference: chr 4
allele count: 1
allele frequency: 8.415949908266146e-6
allele num: 118822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*229C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1301C>T
  hgvsp: ENST00000514940.1:c.1301C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2091C>T
  hgvsp: ENST00000446856.1:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*229C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*229C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2184C>T
  hgvsp: ENST00000264758.7:c.2184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1905C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*229C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2091C>T
  hgvsp: ENST00000398129.1:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*229C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*116C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val728Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-2930127-CGAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930127
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930124
    reference: chr 4
allele count: 1
allele frequency: 8.415949908266146e-6
allele num: 118822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1910_1912delAGG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2189_2191delAGG
  hgvsp: ENSP00000264758.6:p.Glu730del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*234_*236delAGG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*234_*236delAGG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2096_2098delAGG
  hgvsp: ENSP00000381197.1:p.Glu699del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*234_*236delAGG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*234_*236delAGG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2096_2098delAGG
  hgvsp: ENSP00000399828.1:p.Glu699del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*121_*123delAGG
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1306_1308delAGG
  hgvsp: ENSP00000424143.1:p.Glu436del
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*234_*236delAGG
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu730del
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: CGAG
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

4-2930128-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930128
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930128
    reference: chr 4
allele count: 1
allele frequency: 8.409863087428936e-6
allele num: 118908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*117G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2092G>A
  hgvsp: ENSP00000381197.1:p.Glu698Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*230G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*230G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*230G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2185G>A
  hgvsp: ENSP00000264758.6:p.Glu729Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2092G>A
  hgvsp: ENSP00000399828.1:p.Glu698Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1302G>A
  hgvsp: ENSP00000424143.1:p.Glu435Lys
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*230G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1906G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*230G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11178
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu729Lys
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

4-2930128-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930128
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930128
    reference: chr 4
allele count: 1
allele frequency: 8.409863087428936e-6
allele num: 118908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*230G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2092G>C
  hgvsp: ENSP00000381197.1:p.Glu698Gln
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2185G>C
  hgvsp: ENSP00000264758.6:p.Glu729Gln
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1302G>C
  hgvsp: ENSP00000424143.1:p.Glu435Gln
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*230G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2092G>C
  hgvsp: ENSP00000399828.1:p.Glu698Gln
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*230G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*230G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*230G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1906G>C
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*117G>C
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu729Gln
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

4-2930130-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930130
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930130
    reference: chr 4
allele count: 1
allele frequency: 8.407600470825626e-6
allele num: 118940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*232G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*119G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2094G>A
  hgvsp: ENST00000398129.1:c.2094G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*232G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2094G>A
  hgvsp: ENST00000446856.1:c.2094G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1304G>A
  hgvsp: ENST00000514940.1:c.1304G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*232G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2187G>A
  hgvsp: ENST00000264758.7:c.2187G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*232G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*232G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1908G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu729Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

4-2930139-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930139
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930139
    reference: chr 4
allele count: 4
allele frequency: 3.354297693920335e-5
allele num: 119250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*241C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1917C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*128C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2103C>T
  hgvsp: ENST00000446856.1:c.2103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2103C>T
  hgvsp: ENST00000398129.1:c.2103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*241C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*241C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1313C>T
  hgvsp: ENST00000514940.1:c.1313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2196C>T
  hgvsp: ENST00000264758.7:c.2196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*241C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*241C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Ala732Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-2930140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930140
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930140
    reference: chr 4
allele count: 1
allele frequency: 8.381948635418762e-6
allele num: 119304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1314G>A
  hgvsp: ENSP00000424143.1:p.Ala439Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2197G>A
  hgvsp: ENSP00000264758.6:p.Ala733Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*242G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*242G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1918G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2104G>A
  hgvsp: ENSP00000399828.1:p.Ala702Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*242G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*242G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*242G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*129G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2104G>A
  hgvsp: ENSP00000381197.1:p.Ala702Thr
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11245
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala733Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

4-2930142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930142
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930142
    reference: chr 4
allele count: 2
allele frequency: 1.675547066117087e-5
allele num: 119364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*244C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2199C>T
  hgvsp: ENST00000264758.7:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*244C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*244C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*244C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2106C>T
  hgvsp: ENST00000446856.1:c.2106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*244C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1920C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*131C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1316C>T
  hgvsp: ENST00000514940.1:c.1316C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2106C>T
  hgvsp: ENST00000398129.1:c.2106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala733Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

4-2930143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930143
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930143
    reference: chr 4
allele count: 5
allele frequency: 4.186763129689175e-5
allele num: 119424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1317G>A
  hgvsp: ENSP00000424143.1:p.Ala440Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2107G>A
  hgvsp: ENSP00000399828.1:p.Ala703Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*245G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2200G>A
  hgvsp: ENSP00000264758.6:p.Ala734Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*132G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1921G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2107G>A
  hgvsp: ENSP00000381197.1:p.Ala703Thr
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*245G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*245G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*245G>A
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*245G>A
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala734Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

4-2930144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2930144
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 2930144
    reference: chr 4
allele count: 22
allele frequency: 1.841805639273994e-4
allele num: 119448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000424143
  ensembl transcript: ENST00000514940
  gene symbol: ADD1
  hgvsc: ENST00000514940.1:c.1318C>T
  hgvsp: ENSP00000424143.1:p.Ala440Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000264758
  ensembl transcript: ENST00000264758
  gene symbol: ADD1
  hgvsc: ENST00000264758.7:c.2201C>T
  hgvsp: ENSP00000264758.6:p.Ala734Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000087274
  ensembl transcript: ENST00000513762
  gene symbol: ADD1
  hgvsc: ENST00000513762.1:n.1922C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381191
  ensembl transcript: ENST00000398123
  gene symbol: ADD1
  hgvsc: ENST00000398123.2:c.*246C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381197
  ensembl transcript: ENST00000398129
  gene symbol: ADD1
  hgvsc: ENST00000398129.1:c.2108C>T
  hgvsp: ENSP00000381197.1:p.Ala703Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000438069
  ensembl transcript: ENST00000536424
  gene symbol: ADD1
  hgvsc: ENST00000536424.1:c.*133C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000399828
  ensembl transcript: ENST00000446856
  gene symbol: ADD1
  hgvsc: ENST00000446856.1:c.2108C>T
  hgvsp: ENSP00000399828.1:p.Ala703Val
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000348100
  ensembl transcript: ENST00000355842
  gene symbol: ADD1
  hgvsc: ENST00000355842.3:c.*246C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000421907
  ensembl transcript: ENST00000513328
  gene symbol: ADD1
  hgvsc: ENST00000513328.2:c.*246C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000423024
  ensembl transcript: ENST00000503455
  gene symbol: ADD1
  hgvsc: ENST00000503455.2:c.*246C>T
  variant of: http://identifiers.org/hgnc/243
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000087274
  ensembl protein: ENSP00000381193
  ensembl transcript: ENST00000398125
  gene symbol: ADD1
  hgvsc: ENST00000398125.1:c.*246C>T
  variant of: http://identifiers.org/hgnc/243
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala734Val
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1271
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4052
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 4737
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22715
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13118
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4399
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

FS
type: SiteQuality
SIO_000300: 8.129999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

VQSLOD
type: SiteQuality
SIO_000300: -9.757e-1

DP
type: SiteQuality
SIO_000300: 2.455742e6

GenotypeDepth
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2022
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13123
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3072
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22714
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 4740
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6334
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49288176232579e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.799e0

QD
type: SiteQuality
SIO_000300: 1.08e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

FS
type: SiteQuality
SIO_000300: 1.801e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

MQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

DP
type: SiteQuality
SIO_000300: 2.456473e6

GenotypeDepth
all individuals: 2023
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5679
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7399
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 765
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13122
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6332
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 4398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22709
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4741
bin: 7.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.492e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e0

DP
type: SiteQuality
SIO_000300: 2.454955e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e0

FS
type: SiteQuality
SIO_000300: 3.479e0

QD
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeDepth
all individuals: 448
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7398
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5679
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3070
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3074
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13128
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6335
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22709
bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.454804e6

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.198e0

FS
type: SiteQuality
SIO_000300: 1.684e0

VQSLOD
type: SiteQuality
SIO_000300: 4.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.474e0

QD
type: SiteQuality
SIO_000300: 1.241e1

GenotypeDepth
all individuals: 9627
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7397
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12245
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5680
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13126
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6331
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22710
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

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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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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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MQRankSum
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66738
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East Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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South Asian
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MQRankSum
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MQ
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FS
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66738
num of homozygotes: 0

Latino
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allele num: 11578
num of homozygotes: 0

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

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

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

Latino
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East Asian
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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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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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Other
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African
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Latino
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South Asian
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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DP
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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South Asian
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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QD
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VQSLOD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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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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African
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South Asian
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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South Asian
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MQ
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QD
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MQRankSum
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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FS
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BaseQRankSum
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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African
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European (Non-Finnish)
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Other
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East Asian
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DP
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VQSLOD
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MQ
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QD
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MQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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East Asian
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South Asian
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MQRankSum
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FS
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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FS
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VQSLOD
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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FS
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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European (Finnish)
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allele frequency: 3.023888720895071e-4
allele num: 6614
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Other
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DP
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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MQ
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Other
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Latino
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African
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South Asian
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European (Finnish)
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FS
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

East Asian
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Latino
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African
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European (Finnish)
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South Asian
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Other
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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FS
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QD
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MQ
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ClippingRankSum
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SIO_000300: 8.51e-1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

African
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East Asian
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Other
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European (Finnish)
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Latino
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allele num: 11566
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South Asian
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 51

Latino
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num of homozygotes: 0

South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66636
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African
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Other
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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Latino
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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Latino
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South Asian
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East Asian
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European (Finnish)
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FS
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VQSLOD
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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MQRankSum
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MQ
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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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South Asian
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.010959894014212e-5
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Other
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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FS
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

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

European (Finnish)
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Other
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African
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European (Non-Finnish)
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allele num: 66424
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Latino
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South Asian
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ClippingRankSum
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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QD
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BaseQRankSum
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.51828009231143e-5
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African
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East Asian
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South Asian
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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MQRankSum
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DP
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QD
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GenotypeDepth
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variant carriers: 0

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

Other
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num of homozygotes: 0

Latino
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South Asian
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East Asian
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European (Finnish)
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.519248883352071e-5
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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DP
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

African
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allele num: 9648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.523090045083465e-5
allele num: 65656
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.688e1

VQSLOD
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InbreedingCoeff
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SIO_000300: 8.1e-3

BaseQRankSum
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SIO_000300: 6.25e-1

QD
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SIO_000300: 6.45e0

ReadPosRankSum
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SIO_000300: -1.252e0

MQRankSum
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SIO_000300: -2.815e0

FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.382811e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

East Asian
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allele frequency: 4.664179104477612e-4
allele num: 8576
num of homozygotes: 0

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

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

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

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

Latino
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allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

FS
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SIO_000300: 5.103e0

MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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SIO_000300: -4.977e0

MQ
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SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.7e-1

DP
type: SiteQuality
SIO_000300: 2.381196e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
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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: 11528
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.527183872938302e-5
allele num: 65480
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQRankSum
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SIO_000300: -6.909999999999999e-1

BaseQRankSum
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SIO_000300: -5.583e0

FS
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QD
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MQ
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DP
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ReadPosRankSum
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SIO_000300: -1.05e-1

InbreedingCoeff
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SIO_000300: -1.7e-3

VQSLOD
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SIO_000300: -2.098e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e-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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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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bin: 9.75e1
variant carriers: 4

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.583091447951358e-5
allele num: 65458
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
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SIO_000300: 1.5e-3

MQRankSum
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SIO_000300: 9.26e-1

DP
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SIO_000300: 2.377303e6

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

QD
type: SiteQuality
SIO_000300: 1.372e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.44e0

GenotypeQuality
all individuals: 5606
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2318
bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.528257480820369e-5
allele num: 65434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9478
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.422e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
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SIO_000300: -1.7e-3

ClippingRankSum
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MQRankSum
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FS
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DP
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SIO_000300: 2.377186e6

BaseQRankSum
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SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52849107361213e-5
allele num: 65424
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.71e0

MQ
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: -1.9e-3

ReadPosRankSum
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DP
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MQRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65322
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

MQ
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MQRankSum
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FS
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ClippingRankSum
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QD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.130833155763904e-4
allele num: 9386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 14
allele frequency: 2.150669780017205e-4
allele num: 65096
num of homozygotes: 0

East Asian
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Other
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.531018433461939e-5
allele num: 65316
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
type: SiteQuality
SIO_000300: 5.17e-1

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
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

European (Non-Finnish)
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allele count: 1
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allele num: 65328
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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SIO_000300: 5.957e1

FS
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DP
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SIO_000300: 2.362722e6

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.530971554548516e-5
allele num: 65318
num of homozygotes: 0

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

ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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MQ
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QD
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ClippingRankSum
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SIO_000300: 1.83e0

MQRankSum
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

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

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

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

Other
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allele frequency: 0.0e0
allele num: 896
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

European (Non-Finnish)
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allele count: 1
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allele num: 65294
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 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

African
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allele frequency: 1.060670343657191e-4
allele num: 9428
num of homozygotes: 0

European (Finnish)
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DP
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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South Asian
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allele num: 16490
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Latino
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num of homozygotes: 0

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

South Asian
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Latino
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allele num: 11540
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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Latino
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East Asian
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European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65552
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South Asian
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allele num: 16496
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European (Finnish)
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African
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Latino
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East Asian
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Other
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DP
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele num: 9566
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South Asian
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Latino
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ReadPosRankSum
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FS
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MQRankSum
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DP
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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European (Finnish)
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Latino
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South Asian
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African
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.615682212812623e-5
allele num: 65654
num of homozygotes: 0

Latino
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South Asian
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East Asian
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Other
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QD
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VQSLOD
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FS
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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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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