16-4751026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751026
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751026
    reference: chr 16
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1229G>A
  hgvsp: ENSP00000304586.4:p.Gly410Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.908G>A
  hgvsp: ENSP00000466228.1:p.Gly303Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1683G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.1010G>A
  hgvsp: ENSP00000465294.1:p.Gly337Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.710G>A
  hgvsp: ENSP00000468234.1:p.Gly237Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*583G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*684G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.297G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.842G>A
  hgvsp: ENSP00000406796.2:p.Gly281Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.611G>A
  hgvsp: ENSP00000388270.2:p.Gly204Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1960G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*844G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1077G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly410Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

16-4751035-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751035
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751035
    reference: chr 16
allele count: 162
allele frequency: 1.335884157403437e-3
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1068A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.602A>G
  hgvsp: ENSP00000388270.2:p.Asp201Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.1001A>G
  hgvsp: ENSP00000465294.1:p.Asp334Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.701A>G
  hgvsp: ENSP00000468234.1:p.Asp234Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1951A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.899A>G
  hgvsp: ENSP00000466228.1:p.Asp300Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.288A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*835A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1220A>G
  hgvsp: ENSP00000304586.4:p.Asp407Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*574A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.833A>G
  hgvsp: ENSP00000406796.2:p.Asp278Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1674A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*675A>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39455
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Asp407Gly
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

16-4751038-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751038
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751038
    reference: chr 16
allele count: 3
allele frequency: 2.47390035129385e-5
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1671C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.285C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.830C>T
  hgvsp: ENSP00000406796.2:p.Thr277Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1065C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1217C>T
  hgvsp: ENSP00000304586.4:p.Thr406Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*571C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.698C>T
  hgvsp: ENSP00000468234.1:p.Thr233Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*832C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1948C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*672C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.599C>T
  hgvsp: ENSP00000388270.2:p.Thr200Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.998C>T
  hgvsp: ENSP00000465294.1:p.Thr333Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.896C>T
  hgvsp: ENSP00000466228.1:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr406Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

16-4751039-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751039
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751039
    reference: chr 16
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.697A>G
  hgvsp: ENSP00000468234.1:p.Thr233Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1670A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*831A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*671A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.895A>G
  hgvsp: ENSP00000466228.1:p.Thr299Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1064A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.598A>G
  hgvsp: ENSP00000388270.2:p.Thr200Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.997A>G
  hgvsp: ENSP00000465294.1:p.Thr333Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1216A>G
  hgvsp: ENSP00000304586.4:p.Thr406Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1947A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.284A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.829A>G
  hgvsp: ENSP00000406796.2:p.Thr277Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*570A>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr406Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

16-4751044-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751044
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751044
    reference: chr 16
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*666C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.692C>G
  hgvsp: ENSP00000468234.1:p.Ala231Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.824C>G
  hgvsp: ENSP00000406796.2:p.Ala275Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1942C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.593C>G
  hgvsp: ENSP00000388270.2:p.Ala198Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*826C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.992C>G
  hgvsp: ENSP00000465294.1:p.Ala331Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1211C>G
  hgvsp: ENSP00000304586.4:p.Ala404Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1059C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1665C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*565C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.279C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.890C>G
  hgvsp: ENSP00000466228.1:p.Ala297Gly
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala404Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

16-4751044-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751044
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751044
    reference: chr 16
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.593C>A
  hgvsp: ENSP00000388270.2:p.Ala198Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1211C>A
  hgvsp: ENSP00000304586.4:p.Ala404Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.824C>A
  hgvsp: ENSP00000406796.2:p.Ala275Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*826C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*666C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.890C>A
  hgvsp: ENSP00000466228.1:p.Ala297Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.992C>A
  hgvsp: ENSP00000465294.1:p.Ala331Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.692C>A
  hgvsp: ENSP00000468234.1:p.Ala231Asp
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.279C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1665C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1059C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1942C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*565C>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39430
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala404Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

16-4751045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751045
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751045
    reference: chr 16
allele count: 64744
allele frequency: 5.336454452540306e-1
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1210G>A
  hgvsp: ENSP00000304586.4:p.Ala404Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*665G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*564G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1941G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.889G>A
  hgvsp: ENSP00000466228.1:p.Ala297Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.823G>A
  hgvsp: ENSP00000406796.2:p.Ala275Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.691G>A
  hgvsp: ENSP00000468234.1:p.Ala231Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.991G>A
  hgvsp: ENSP00000465294.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.592G>A
  hgvsp: ENSP00000388270.2:p.Ala198Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1664G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*825G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.278G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1058G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 3.25e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.75e1
  variant carriers: 357
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 521
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.75e1
  variant carriers: 380
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 2.75e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 652
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 681
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 2.25e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 40275
  bin: 9.75e1
  variant carriers: 40267
genotype quality: GenotypeQuality
hgvs: p.Ala404Thr
num of homozygotes: 17578
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

16-4751046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751046
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751046
    reference: chr 16
allele count: 4
allele frequency: 3.301092661671013e-5
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.277C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.822C>T
  hgvsp: ENST00000446014.2:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1057C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*664C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.990C>T
  hgvsp: ENST00000585773.1:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1209C>T
  hgvsp: ENST00000304283.4:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.690C>T
  hgvsp: ENST00000586605.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.591C>T
  hgvsp: ENST00000450067.2:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.888C>T
  hgvsp: ENST00000592421.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*563C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*824C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1663C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1940C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg403Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

16-4751047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751047
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751047
    reference: chr 16
allele count: 31
allele frequency: 2.55843126898191e-4
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.887G>A
  hgvsp: ENSP00000466228.1:p.Arg296His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*823G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1056G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.689G>A
  hgvsp: ENSP00000468234.1:p.Arg230His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.590G>A
  hgvsp: ENSP00000388270.2:p.Arg197His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1939G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.276G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1662G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*562G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1208G>A
  hgvsp: ENSP00000304586.4:p.Arg403His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.821G>A
  hgvsp: ENSP00000406796.2:p.Arg274His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.989G>A
  hgvsp: ENSP00000465294.1:p.Arg330His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*663G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg403His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-4751048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751048
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751048
    reference: chr 16
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.688C>T
  hgvsp: ENSP00000468234.1:p.Arg230Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*662C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.820C>T
  hgvsp: ENSP00000406796.2:p.Arg274Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1661C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.589C>T
  hgvsp: ENSP00000388270.2:p.Arg197Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*561C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.886C>T
  hgvsp: ENSP00000466228.1:p.Arg296Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.275C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1207C>T
  hgvsp: ENSP00000304586.4:p.Arg403Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.988C>T
  hgvsp: ENSP00000465294.1:p.Arg330Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1938C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1055C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*822C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg403Cys
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-4751049-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751049
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751049
    reference: chr 16
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.885C>T
  hgvsp: ENST00000592421.1:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*821C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.819C>T
  hgvsp: ENST00000446014.2:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.588C>T
  hgvsp: ENST00000450067.2:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.274C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1206C>T
  hgvsp: ENST00000304283.4:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*560C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1660C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1054C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.987C>T
  hgvsp: ENST00000585773.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1937C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.687C>T
  hgvsp: ENST00000586605.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*661C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro402Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

16-4751051-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751051
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751051
    reference: chr 16
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1204C>T
  hgvsp: ENSP00000304586.4:p.Pro402Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1658C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.817C>T
  hgvsp: ENSP00000406796.2:p.Pro273Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*659C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*558C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1052C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*819C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.883C>T
  hgvsp: ENSP00000466228.1:p.Pro295Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.272C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1935C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.685C>T
  hgvsp: ENSP00000468234.1:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.985C>T
  hgvsp: ENSP00000465294.1:p.Pro329Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.586C>T
  hgvsp: ENSP00000388270.2:p.Pro196Ser
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro402Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-4751051-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751051
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751051
    reference: chr 16
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.685C>G
  hgvsp: ENSP00000468234.1:p.Pro229Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*819C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1658C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.817C>G
  hgvsp: ENSP00000406796.2:p.Pro273Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.272C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.883C>G
  hgvsp: ENSP00000466228.1:p.Pro295Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.586C>G
  hgvsp: ENSP00000388270.2:p.Pro196Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1935C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1052C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1204C>G
  hgvsp: ENSP00000304586.4:p.Pro402Ala
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*558C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*659C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.985C>G
  hgvsp: ENSP00000465294.1:p.Pro329Ala
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro402Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

16-4751053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751053
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751053
    reference: chr 16
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*556C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*817C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.815C>T
  hgvsp: ENSP00000406796.2:p.Pro272Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.270C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1656C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.881C>T
  hgvsp: ENSP00000466228.1:p.Pro294Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1933C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.683C>T
  hgvsp: ENSP00000468234.1:p.Pro228Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.584C>T
  hgvsp: ENSP00000388270.2:p.Pro195Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1202C>T
  hgvsp: ENSP00000304586.4:p.Pro401Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*657C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*231C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.983C>T
  hgvsp: ENSP00000465294.1:p.Pro328Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1050C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro401Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

16-4751054-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751054
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751054
    reference: chr 16
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.269C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.982C>A
  hgvsp: ENSP00000465294.1:p.Pro328Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1655C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.880C>A
  hgvsp: ENSP00000466228.1:p.Pro294Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1932C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.583C>A
  hgvsp: ENSP00000388270.2:p.Pro195Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*555C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.814C>A
  hgvsp: ENSP00000406796.2:p.Pro272Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1201C>A
  hgvsp: ENSP00000304586.4:p.Pro401Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.682C>A
  hgvsp: ENSP00000468234.1:p.Pro228Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*816C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*230C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1049C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*656C>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro401Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-4751058-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751058
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751058
    reference: chr 16
allele count: 3
allele frequency: 2.476596166229135e-5
allele num: 121134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.265G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*812G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.810G>C
  hgvsp: ENSP00000406796.2:p.Gln270His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1928G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*551G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.678G>C
  hgvsp: ENSP00000468234.1:p.Gln226His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*652G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.579G>C
  hgvsp: ENSP00000388270.2:p.Gln193His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1197G>C
  hgvsp: ENSP00000304586.4:p.Gln399His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1651G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.876G>C
  hgvsp: ENSP00000466228.1:p.Gln292His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.978G>C
  hgvsp: ENSP00000465294.1:p.Gln326His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1045G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*226G>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln399His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-4751061-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751061
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751061
    reference: chr 16
allele count: 3
allele frequency: 2.476882430647292e-5
allele num: 121120
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1194C>T
  hgvsp: ENST00000304283.4:c.1194C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*548C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.807C>T
  hgvsp: ENST00000446014.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1925C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1648C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*649C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*809C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.675C>T
  hgvsp: ENST00000586605.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.873C>T
  hgvsp: ENST00000592421.1:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.576C>T
  hgvsp: ENST00000450067.2:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*223C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.975C>T
  hgvsp: ENST00000585773.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.262C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1042C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser398Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-4751061-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751061
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751061
    reference: chr 16
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.807C>A
  hgvsp: ENSP00000406796.2:p.Ser269Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1648C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.576C>A
  hgvsp: ENSP00000388270.2:p.Ser192Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*223C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*649C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.873C>A
  hgvsp: ENSP00000466228.1:p.Ser291Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.675C>A
  hgvsp: ENSP00000468234.1:p.Ser225Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1194C>A
  hgvsp: ENSP00000304586.4:p.Ser398Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1925C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*809C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1042C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*548C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.975C>A
  hgvsp: ENSP00000465294.1:p.Ser325Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.262C>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser398Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/16-4751062-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751062
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751062
    reference: chr 16
allele count: 1
allele frequency: 8.256138438929344e-6
allele num: 121122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*222G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1041G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.575G>T
  hgvsp: ENSP00000388270.2:p.Ser192Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*808G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1924G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1193G>T
  hgvsp: ENSP00000304586.4:p.Ser398Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*547G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*648G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.806G>T
  hgvsp: ENSP00000406796.2:p.Ser269Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.872G>T
  hgvsp: ENSP00000466228.1:p.Ser291Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.974G>T
  hgvsp: ENSP00000465294.1:p.Ser325Ile
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1647G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.261G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.674G>T
  hgvsp: ENSP00000468234.1:p.Ser225Ile
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser398Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

16-4751066-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751066
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751066
    reference: chr 16
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.802G>C
  hgvsp: ENSP00000406796.2:p.Asp268His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.571G>C
  hgvsp: ENSP00000388270.2:p.Asp191His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.670G>C
  hgvsp: ENSP00000468234.1:p.Asp224His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1920G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1037G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1189G>C
  hgvsp: ENSP00000304586.4:p.Asp397His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*644G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.868G>C
  hgvsp: ENSP00000466228.1:p.Asp290His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.970G>C
  hgvsp: ENSP00000465294.1:p.Asp324His
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*218G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*543G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*804G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.257G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1643G>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp397His
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

16-4751075-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751075
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751075
    reference: chr 16
allele count: 3
allele frequency: 2.478478544637399e-5
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.562A>G
  hgvsp: ENSP00000388270.2:p.Lys188Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*209A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*534A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.793A>G
  hgvsp: ENSP00000406796.2:p.Lys265Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.248A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*635A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.859A>G
  hgvsp: ENSP00000466228.1:p.Lys287Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*795A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1028A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1911A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1180A>G
  hgvsp: ENSP00000304586.4:p.Lys394Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.661A>G
  hgvsp: ENSP00000468234.1:p.Lys221Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.961A>G
  hgvsp: ENSP00000465294.1:p.Lys321Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1634A>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys394Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

16-4751095-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751095
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751095
    reference: chr 16
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*775C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.773C>G
  hgvsp: ENSP00000406796.2:p.Ala258Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.542C>G
  hgvsp: ENSP00000388270.2:p.Ala181Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1160C>G
  hgvsp: ENSP00000304586.4:p.Ala387Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.228C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*615C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1614C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.641C>G
  hgvsp: ENSP00000468234.1:p.Ala214Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1008C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*189C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.839C>G
  hgvsp: ENSP00000466228.1:p.Ala280Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.941C>G
  hgvsp: ENSP00000465294.1:p.Ala314Gly
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*514C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1891C>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala387Gly
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

16-4751096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751096
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751096
    reference: chr 16
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.640G>A
  hgvsp: ENSP00000468234.1:p.Ala214Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1007G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1613G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*774G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.541G>A
  hgvsp: ENSP00000388270.2:p.Ala181Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1159G>A
  hgvsp: ENSP00000304586.4:p.Ala387Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.838G>A
  hgvsp: ENSP00000466228.1:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*513G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.772G>A
  hgvsp: ENSP00000406796.2:p.Ala258Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.940G>A
  hgvsp: ENSP00000465294.1:p.Ala314Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.227G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*188G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*614G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1890G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala387Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

16-4751099-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751099
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751099
    reference: chr 16
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.769C>G
  hgvsp: ENSP00000406796.2:p.Gln257Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1887C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1610C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.937C>G
  hgvsp: ENSP00000465294.1:p.Gln313Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.637C>G
  hgvsp: ENSP00000468234.1:p.Gln213Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*611C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1156C>G
  hgvsp: ENSP00000304586.4:p.Gln386Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.224C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*185C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.835C>G
  hgvsp: ENSP00000466228.1:p.Gln279Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.538C>G
  hgvsp: ENSP00000388270.2:p.Gln180Glu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*771C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*510C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1004C>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln386Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

16-4751101-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751101
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751101
    reference: chr 16
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*183A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.222A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1154A>C
  hgvsp: ENSP00000304586.4:p.Lys385Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*508A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.635A>C
  hgvsp: ENSP00000468234.1:p.Lys212Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1608A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.767A>C
  hgvsp: ENSP00000406796.2:p.Lys256Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.833A>C
  hgvsp: ENSP00000466228.1:p.Lys278Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1885A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*769A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*609A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.935A>C
  hgvsp: ENSP00000465294.1:p.Lys312Thr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1002A>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.536A>C
  hgvsp: ENSP00000388270.2:p.Lys179Thr
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys385Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

16-4751103-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751103
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751103
    reference: chr 16
allele count: 4
allele frequency: 3.312519668085529e-5
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.633C>T
  hgvsp: ENST00000586605.1:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*181C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*767C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.933C>T
  hgvsp: ENST00000585773.1:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1883C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1152C>T
  hgvsp: ENST00000304283.4:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.831C>T
  hgvsp: ENST00000592421.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.765C>T
  hgvsp: ENST00000446014.2:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.534C>T
  hgvsp: ENST00000450067.2:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1606C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.220C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*506C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+1000C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*607C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg384Arg
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-4751105-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751105
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751105
    reference: chr 16
allele count: 3
allele frequency: 2.484718978283556e-5
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*765C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.218C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*605C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.931C>T
  hgvsp: ENSP00000465294.1:p.Arg311Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+998C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.763C>T
  hgvsp: ENSP00000406796.2:p.Arg255Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1150C>T
  hgvsp: ENSP00000304586.4:p.Arg384Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*504C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*179C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1881C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.829C>T
  hgvsp: ENSP00000466228.1:p.Arg277Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.631C>T
  hgvsp: ENSP00000468234.1:p.Arg211Cys
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1604C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.532C>T
  hgvsp: ENSP00000388270.2:p.Arg178Cys
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg384Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

16-4751107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751107
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751107
    reference: chr 16
allele count: 1
allele frequency: 8.283768783445716e-6
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.761C>T
  hgvsp: ENSP00000406796.2:p.Ala254Val
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.530C>T
  hgvsp: ENSP00000388270.2:p.Ala177Val
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*177C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+996C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1148C>T
  hgvsp: ENSP00000304586.4:p.Ala383Val
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.629C>T
  hgvsp: ENSP00000468234.1:p.Ala210Val
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.827C>T
  hgvsp: ENSP00000466228.1:p.Ala276Val
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.216C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*763C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.929C>T
  hgvsp: ENSP00000465294.1:p.Ala310Val
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1602C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1879C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*502C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*603C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala383Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

16-4751110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751110
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751110
    reference: chr 16
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1145C>T
  hgvsp: ENSP00000304586.4:p.Ser382Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1876C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.626C>T
  hgvsp: ENSP00000468234.1:p.Ser209Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*600C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.758C>T
  hgvsp: ENSP00000406796.2:p.Ser253Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.824C>T
  hgvsp: ENSP00000466228.1:p.Ser275Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.926C>T
  hgvsp: ENSP00000465294.1:p.Ser309Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*174C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.527C>T
  hgvsp: ENSP00000388270.2:p.Ser176Leu
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1599C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*499C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.213C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+993C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser382Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

16-4751118-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751118
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751118
    reference: chr 16
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*752T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.816T>C
  hgvsp: ENST00000592421.1:c.816T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.750T>C
  hgvsp: ENST00000446014.2:c.750T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1591T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.918T>C
  hgvsp: ENST00000585773.1:c.918T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.205T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1137T>C
  hgvsp: ENST00000304283.4:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*592T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.519T>C
  hgvsp: ENST00000450067.2:c.519T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*491T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.618T>C
  hgvsp: ENST00000586605.1:c.618T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1868T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+985T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*166T>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys379Cys
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

16-4751119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751119
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751119
    reference: chr 16
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.749G>A
  hgvsp: ENSP00000406796.2:p.Cys250Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1590G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*490G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*165G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1867G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1136G>A
  hgvsp: ENSP00000304586.4:p.Cys379Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.815G>A
  hgvsp: ENSP00000466228.1:p.Cys272Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+984G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*751G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.617G>A
  hgvsp: ENSP00000468234.1:p.Cys206Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.917G>A
  hgvsp: ENSP00000465294.1:p.Cys306Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.518G>A
  hgvsp: ENSP00000388270.2:p.Cys173Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.204G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.518G>A
  hgvsp: ENST00000586166.1:c.518G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*591G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys379Tyr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-4751123-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751123
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751123
    reference: chr 16
allele count: 1
allele frequency: 8.30357884248111e-6
allele num: 120430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.745G>T
  hgvsp: ENSP00000406796.2:p.Ala249Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.514G>T
  hgvsp: ENSP00000388270.2:p.Ala172Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*486G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*747G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*587G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.200G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.913G>T
  hgvsp: ENSP00000465294.1:p.Ala305Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1863G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*161G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.811G>T
  hgvsp: ENSP00000466228.1:p.Ala271Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1132G>T
  hgvsp: ENSP00000304586.4:p.Ala378Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.514G>T
  hgvsp: ENSP00000465373.1:p.Ala172Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.613G>T
  hgvsp: ENSP00000468234.1:p.Ala205Ser
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1586G>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+980G>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala378Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

16-4751124-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751124
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751124
    reference: chr 16
allele count: 703
allele frequency: 5.837512870760952e-3
allele num: 120428
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.199T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.513T>C
  hgvsp: ENST00000450067.2:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1131T>C
  hgvsp: ENST00000304283.4:c.1131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*746T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.912T>C
  hgvsp: ENST00000585773.1:c.912T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1585T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.612T>C
  hgvsp: ENST00000586605.1:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.513T>C
  hgvsp: ENST00000586166.1:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+979T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*485T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.744T>C
  hgvsp: ENST00000446014.2:c.744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.810T>C
  hgvsp: ENST00000592421.1:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*586T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1862T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*160T>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.His377His
num of homozygotes: 21
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

16-4751125-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751125
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751125
    reference: chr 16
allele count: 1
allele frequency: 8.306061763875276e-6
allele num: 120394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*745A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.611A>G
  hgvsp: ENSP00000468234.1:p.His204Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.198A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*159A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.512A>G
  hgvsp: ENSP00000465373.1:p.His171Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1861A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+978A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*585A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.911A>G
  hgvsp: ENSP00000465294.1:p.His304Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1584A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*484A>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.512A>G
  hgvsp: ENSP00000388270.2:p.His171Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.743A>G
  hgvsp: ENSP00000406796.2:p.His248Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1130A>G
  hgvsp: ENSP00000304586.4:p.His377Arg
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.809A>G
  hgvsp: ENSP00000466228.1:p.His270Arg
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His377Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

16-4751126-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751126
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751126
    reference: chr 16
allele count: 4
allele frequency: 3.322700691121744e-5
allele num: 120384
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1129C>T
  hgvsp: ENSP00000304586.4:p.His377Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.610C>T
  hgvsp: ENSP00000468234.1:p.His204Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.808C>T
  hgvsp: ENSP00000466228.1:p.His270Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*483C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1583C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*584C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*158C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.910C>T
  hgvsp: ENSP00000465294.1:p.His304Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.511C>T
  hgvsp: ENSP00000465373.1:p.His171Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.197C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1860C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.511C>T
  hgvsp: ENSP00000388270.2:p.His171Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.742C>T
  hgvsp: ENSP00000406796.2:p.His248Tyr
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+977C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*744C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His377Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

16-4751132-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751132
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751132
    reference: chr 16
allele count: 1
allele frequency: 8.313104778372627e-6
allele num: 120292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.736T>C
  hgvsp: ENSP00000406796.2:p.Ser246Pro
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*578T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.604T>C
  hgvsp: ENSP00000468234.1:p.Ser202Pro
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+971T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.904T>C
  hgvsp: ENSP00000465294.1:p.Ser302Pro
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.191T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1123T>C
  hgvsp: ENSP00000304586.4:p.Ser375Pro
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.802T>C
  hgvsp: ENSP00000466228.1:p.Ser268Pro
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*477T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.505T>C
  hgvsp: ENSP00000388270.2:p.Ser169Pro
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.505T>C
  hgvsp: ENSP00000465373.1:p.Ser169Pro
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1854T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*152T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*738T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1577T>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser375Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-4751135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751135
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751135
    reference: chr 16
allele count: 1
allele frequency: 8.316008316008316e-6
allele num: 120250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901G>A
  hgvsp: ENSP00000465294.1:p.Asp301Asn
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502G>A
  hgvsp: ENSP00000465373.1:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+968G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120G>A
  hgvsp: ENSP00000304586.4:p.Asp374Asn
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601G>A
  hgvsp: ENSP00000468234.1:p.Asp201Asn
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502G>A
  hgvsp: ENSP00000388270.2:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733G>A
  hgvsp: ENSP00000406796.2:p.Asp245Asn
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799G>A
  hgvsp: ENSP00000466228.1:p.Asp267Asn
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp374Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4751147-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751147
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751147
    reference: chr 16
allele count: 2
allele frequency: 1.666805567130594e-5
allele num: 119990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+956C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-12C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-12C>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4751148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751148
    reference: chr 16
allele count: 3
allele frequency: 2.501250625312656e-5
allele num: 119940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+955C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-13C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-13C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-4751148-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751148
    reference: chr 16
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+955C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-13C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-13C>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-4751148-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751148
    reference: chr 16
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-13C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+955C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-13C>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

16-4751150-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751150
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751150
    reference: chr 16
allele count: 3
allele frequency: 2.501834678764427e-5
allele num: 119912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+953C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-15C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-15C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

16-4751153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751153
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751153
    reference: chr 16
allele count: 1
allele frequency: 8.341814177747376e-6
allele num: 119878
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+950G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-18G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-18G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-4751154-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751154
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751154
    reference: chr 16
allele count: 1
allele frequency: 8.34306691139663e-6
allele num: 119860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+949T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-19T>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

16-4751164-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751164
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751164
    reference: chr 16
allele count: 1
allele frequency: 8.363861427543869e-6
allele num: 119562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+939C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-29C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-29C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

16-4751167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751167
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751167
    reference: chr 16
allele count: 11
allele frequency: 9.211341673784522e-5
allele num: 119418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+936G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-32G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-32G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

16-4751168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751168
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751168
    reference: chr 16
allele count: 1
allele frequency: 8.373946976167747e-6
allele num: 119418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+935C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-33C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-4751169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751169
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751169
    reference: chr 16
allele count: 4
allele frequency: 3.350757271143279e-5
allele num: 119376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-34G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+934G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-34G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4751172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751172
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751172
    reference: chr 16
allele count: 2
allele frequency: 1.676951972095519e-5
allele num: 119264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+931C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-37C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-37C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

16-4751178-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751178
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751178
    reference: chr 16
allele count: 2
allele frequency: 1.682170673036486e-5
allele num: 118894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+925A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-43A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-43A>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-4751180-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751180
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751180
    reference: chr 16
allele count: 1
allele frequency: 8.414675193537529e-6
allele num: 118840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-45C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+923C>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

16-4751184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751184
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751184
    reference: chr 16
allele count: 9
allele frequency: 7.593526940146133e-5
allele num: 118522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*575-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*735-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.901-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.799-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1851-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.733-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+919C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.601-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1574-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*149-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*474-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.188-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.502-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.502-49C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1120-49C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5784
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

16-4751384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751384
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751384
    reference: chr 16
allele count: 2
allele frequency: 2.70175343798125e-5
allele num: 74026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+719G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+51G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+51G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21548
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-4751386-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751386
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751386
    reference: chr 16
allele count: 2
allele frequency: 2.684563758389262e-5
allele num: 74500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+717A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+49A>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+49A>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

16-4751388-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751388
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751388
    reference: chr 16
allele count: 2
allele frequency: 2.689979825151311e-5
allele num: 74350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+715G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+47G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+47G>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21595
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-4751397-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751397
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751397
    reference: chr 16
allele count: 1
allele frequency: 1.318044022670357e-5
allele num: 75870
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+706C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+38C>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+38C>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-4751400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751400
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751400
    reference: chr 16
allele count: 240
allele frequency: 3.15955766192733e-3
allele num: 75960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+703G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+35G>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+35G>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19249
  bin: 7.5e0
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21192
  bin: 1.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

16-4751402-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751402
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751402
    reference: chr 16
allele count: 2
allele frequency: 2.591210613598673e-5
allele num: 77184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+33C>T
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+701C>T
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20566
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

16-4751407-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751407
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751407
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 78428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+696C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+28C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+28C>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19148
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

16-4751410-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751410
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751410
    reference: chr 16
allele count: 105
allele frequency: 1.30671777385071e-3
allele num: 80354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+693T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+25T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+25T>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17355
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18746
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13965
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4751414-CAAGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751410
    reference: chr 16
allele count: 1
allele frequency: 1.209599380685117e-5
allele num: 82672
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+17_*574+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+17_1119+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+17_1573+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+17_732+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+17_798+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+17_*473+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+17_501+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+17_501+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+17_1850+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+17_*734+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+17_900+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+685_277+688delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+17_187+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+17_600+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+17_*148+20delTCTT
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17787
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: CAAGA
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

16-4751414-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751414
    reference: chr 16
allele count: 1
allele frequency: 1.209599380685117e-5
allele num: 82672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+689G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+21G>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+21G>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17787
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

16-4751416-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751416
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751416
    reference: chr 16
allele count: 1
allele frequency: 1.181558239005601e-5
allele num: 84634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+19T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+687T>C
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+19T>C
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13640
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/16-4751419-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751419
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751419
    reference: chr 16
allele count: 1
allele frequency: 1.14056298188786e-5
allele num: 87676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+684T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+16T>G
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+16T>G
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

16-4751421-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4751421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4751421
    reference: chr 16
allele count: 3
allele frequency: 3.364435671989951e-5
allele num: 89168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465294
  ensembl transcript: ENST00000585773
  gene symbol: ANKS3
  hgvsc: ENST00000585773.1:c.900+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000468234
  ensembl transcript: ENST00000586605
  gene symbol: ANKS3
  hgvsc: ENST00000586605.1:c.600+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465373
  ensembl transcript: ENST00000586166
  gene symbol: ANKS3
  hgvsc: ENST00000586166.1:c.501+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000304586
  ensembl transcript: ENST00000304283
  gene symbol: ANKS3
  hgvsc: ENST00000304283.4:c.1119+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466228
  ensembl transcript: ENST00000592421
  gene symbol: ANKS3
  hgvsc: ENST00000592421.1:c.798+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467591
  ensembl transcript: ENST00000590193
  gene symbol: ANKS3
  hgvsc: ENST00000590193.1:c.*574+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000591653
  gene symbol: ANKS3
  hgvsc: ENST00000591653.1:n.1850+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000590803
  gene symbol: ANKS3
  hgvsc: ENST00000590803.1:n.1573+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465306
  ensembl transcript: ENST00000592068
  gene symbol: ANKS3
  hgvsc: ENST00000592068.1:c.*148+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000465203
  ensembl transcript: ENST00000592077
  gene symbol: ANKS3
  hgvsc: ENST00000592077.1:c.*734+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000466162
  ensembl transcript: ENST00000590730
  gene symbol: ANKS3
  hgvsc: ENST00000590730.1:c.*473+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl transcript: ENST00000592840
  gene symbol: ANKS3
  hgvsc: ENST00000592840.1:n.187+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000388270
  ensembl transcript: ENST00000450067
  gene symbol: ANKS3
  hgvsc: ENST00000450067.2:c.501+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000406796
  ensembl transcript: ENST00000446014
  gene symbol: ANKS3
  hgvsc: ENST00000446014.2:c.732+14C>A
  variant of: http://identifiers.org/hgnc/29422
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168096
  ensembl protein: ENSP00000467439
  ensembl transcript: ENST00000588513
  gene symbol: ANKS3
  hgvsc: ENST00000588513.1:c.277+682C>A
  variant of: http://identifiers.org/hgnc/29422
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25720
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4750
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2399
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2047
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38908
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5256
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 827
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2959
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6896
bin: 6.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.38e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 5.053e0

DP
type: SiteQuality
SIO_000300: 1.997862e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.985e0

GenotypeDepth
all individuals: 99
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 336
bin: 4.75e1
variant carriers: 7

GenotypeDepth
all individuals: 2394
bin: 9.75e1
variant carriers: 127

GenotypeDepth
all individuals: 124
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 275
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 834
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6910
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5281
bin: 9.75e1
variant carriers: 162

GenotypeQuality
all individuals: 2409
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38916
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2973
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.778738115816768e-4
allele num: 11570
num of homozygotes: 0

African
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allele frequency: 1.472286374133949e-2
allele num: 10392
num of homozygotes: 0

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

ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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QD
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InbreedingCoeff
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SIO_000300: 3.9e-3

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.502341217433065e-5
allele num: 66632
num of homozygotes: 0

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

ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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DP
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FS
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InbreedingCoeff
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MQ
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SIO_000300: 5.973e1

BaseQRankSum
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SIO_000300: -7.781e0

VQSLOD
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SIO_000300: 1.14e0

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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bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.858e0

ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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SIO_000300: 9.34e0

MQRankSum
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SIO_000300: 7.37e-1

DP
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SIO_000300: 2.000637e6

InbreedingCoeff
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.686e1

GenotypeDepth
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variant carriers: 0

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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bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

BaseQRankSum
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SIO_000300: -5.3e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
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SIO_000300: 1.42e-1

ClippingRankSum
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SIO_000300: -1.37e0

DP
type: SiteQuality
SIO_000300: 2.001256e6

VQSLOD
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SIO_000300: 3.24e0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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

South 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 count: 0
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num of homozygotes: 0

Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQ
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QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 599

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 780

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: 46877

Latino
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allele count: 5960
allele frequency: 5.149472956626923e-1
allele num: 11574
num of homozygotes: 1551

European (Finnish)
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allele frequency: 5.544464609800362e-1
allele num: 6612
num of homozygotes: 1039

African
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allele frequency: 4.802656911821332e-1
allele num: 10388
num of homozygotes: 1204

South Asian
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allele frequency: 4.669171110033931e-1
allele num: 16504
num of homozygotes: 1876

European (Non-Finnish)
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allele count: 36500
allele frequency: 5.472756169970312e-1
allele num: 66694
num of homozygotes: 10060

East Asian
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allele frequency: 6.271676300578035e-1
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Other
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allele frequency: 5.521064301552107e-1
allele num: 902
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.7e-2

GenotypeDepth
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variant carriers: 3

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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allele count: 0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.64902266043937e-5
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South Asian
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African
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allele count: 0
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European (Finnish)
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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QD
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DP
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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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allele frequency: 0.0e0
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 6.006006006006006e-5
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African
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Latino
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South Asian
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MQ
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66600
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Latino
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European (Finnish)
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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FS
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QD
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MQ
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ReadPosRankSum
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BaseQRankSum
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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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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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East Asian
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European (Non-Finnish)
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South Asian
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African
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Other
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FS
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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QD
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MQ
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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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African
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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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East Asian
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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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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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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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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DP
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QD
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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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 (Non-Finnish)
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European (Finnish)
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South Asian
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East Asian
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Other
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MQ
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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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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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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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66576
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Latino
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South Asian
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African
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East Asian
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Other
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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FS
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MQRankSum
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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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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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

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

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

South Asian
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African
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Other
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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QD
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DP
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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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MQ
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FS
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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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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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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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Other
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East Asian
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South Asian
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InbreedingCoeff
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ClippingRankSum
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FS
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DP
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QD
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MQRankSum
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MQ
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VQSLOD
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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GenotypeQuality
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Latino
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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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East Asian
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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SIO_000300: 2.445359e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505434618974498e-5
allele num: 66426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
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SIO_000300: 1.113e1

MQRankSum
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SIO_000300: 2.12e0

BaseQRankSum
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SIO_000300: -2.469e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

VQSLOD
type: SiteQuality
SIO_000300: -9.340000000000001e-1

DP
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SIO_000300: 2.443125e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 1.165e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505479947007106e-5
allele num: 66424
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 4.257e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.972e0

DP
type: SiteQuality
SIO_000300: 2.443217e6

QD
type: SiteQuality
SIO_000300: 1.287e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.813e0

VQSLOD
type: SiteQuality
SIO_000300: 9.52e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.442681e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.103e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.915e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.441e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

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

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

Other
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VQSLOD
type: SiteQuality
SIO_000300: -5.042e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 8.35e0

BaseQRankSum
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SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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

East Asian
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allele count: 0
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allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 1
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allele num: 894
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.521613311629589e-5
allele num: 66348
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 5.93e1

MQRankSum
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FS
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SIO_000300: 1.222e0

BaseQRankSum
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DP
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QD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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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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: 3

East Asian
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allele count: 2
allele frequency: 2.318034306907742e-4
allele num: 8628
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

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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Other
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66344
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ClippingRankSum
type: SiteQuality
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MQ
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BaseQRankSum
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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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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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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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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South Asian
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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

European (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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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: 1
allele frequency: 1.507522537461935e-5
allele num: 66334
num of homozygotes: 0

East Asian
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BaseQRankSum
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SIO_000300: -1.978e0

VQSLOD
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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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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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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

African
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allele frequency: 9.750390015600624e-5
allele num: 10256
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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ClippingRankSum
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.964e1

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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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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.510300247689241e-5
allele num: 66212
num of homozygotes: 0

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

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

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

South Asian
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num of homozygotes: 0

QD
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ClippingRankSum
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SIO_000300: -7.099999999999999e-2

ReadPosRankSum
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FS
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SIO_000300: 5.84e-1

MQRankSum
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SIO_000300: 2.85e-1

MQ
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InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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SIO_000300: 2.58e0

DP
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SIO_000300: 2.437203e6

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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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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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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

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

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

South Asian
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Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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DP
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VQSLOD
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QD
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FS
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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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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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

African
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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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South Asian
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DP
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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SIO_000300: -3.0e-4

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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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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African
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allele count: 665
allele frequency: 6.517052136417091e-2
allele num: 10204
num of homozygotes: 21

Other
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allele num: 888
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 2.084418968212611e-3
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num of homozygotes: 0

South Asian
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allele frequency: 2.434867299732165e-4
allele num: 16428
num of homozygotes: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.209080192243751e-4
allele num: 66166
num of homozygotes: 0

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

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

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

Latino
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num of homozygotes: 0

African
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Other
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European (Non-Finnish)
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allele num: 65848
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East Asian
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South Asian
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DP
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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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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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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Other
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African
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East Asian
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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DP
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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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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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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African
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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European (Finnish)
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Other
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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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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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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European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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European (Finnish)
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FS
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VQSLOD
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
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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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bin: 9.75e1
variant carriers: 11

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.105565222700491e-5
allele num: 65514
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 7
allele frequency: 4.268292682926829e-4
allele num: 16400
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 3.12e0

ClippingRankSum
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SIO_000300: -6.8e-2

MQ
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SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
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SIO_000300: 5.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

QD
type: SiteQuality
SIO_000300: 1.442e1

DP
type: SiteQuality
SIO_000300: 2.330077e6

GenotypeDepth
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variant carriers: 0

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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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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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526298116548124e-5
allele num: 65518
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

InbreedingCoeff
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SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
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SIO_000300: -2.988e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -1.5e-1

VQSLOD
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SIO_000300: 3.62e0

ReadPosRankSum
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SIO_000300: 4.43e-1

DP
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SIO_000300: 2.329308e6

QD
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GenotypeDepth
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variant carriers: 0

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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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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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.107616197398156e-5
allele num: 65492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

FS
type: SiteQuality
SIO_000300: 2.205e0

VQSLOD
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SIO_000300: 3.15e0

DP
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SIO_000300: 2.326024e6

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

QD
type: SiteQuality
SIO_000300: 1.347e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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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: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.056608387333415e-5
allele num: 65432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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SIO_000300: -1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 2.312268e6

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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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: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.067014261616316e-5
allele num: 65210
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.24e-1

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

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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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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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8564
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

African
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.534636751480924e-5
allele num: 65162
num of homozygotes: 0

South Asian
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MQ
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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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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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allele frequency: 0.0e0
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.051401869158879e-3
allele num: 8560
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South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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MQ
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MQRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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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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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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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.750593824228028e-5
allele num: 42100
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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VQSLOD
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MQRankSum
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FS
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MQ
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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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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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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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 4.723442444853809e-5
allele num: 42342
num of homozygotes: 0

Latino
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -3.06e-1

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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QD
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BaseQRankSum
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

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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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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Latino
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allele frequency: 3.108486167236556e-4
allele num: 6434
num of homozygotes: 0

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

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

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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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

European (Non-Finnish)
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num of homozygotes: 0

Latino
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African
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European (Finnish)
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Other
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 74

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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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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Latino
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allele frequency: 4.507211538461539e-4
allele num: 6656
num of homozygotes: 0

European (Finnish)
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allele frequency: 2.950643776824035e-3
allele num: 3728
num of homozygotes: 0

East Asian
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African
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allele frequency: 1.587759815242494e-3
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South Asian
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allele frequency: 9.009009009009009e-4
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European (Non-Finnish)
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allele frequency: 4.780469692750394e-3
allele num: 43092
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Other
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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QD
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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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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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African
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Other
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East Asian
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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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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East Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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South Asian
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Other
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ClippingRankSum
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DP
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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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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South Asian
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Latino
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East Asian
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African
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European (Non-Finnish)
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allele frequency: 2.004493590025992e-3
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European (Finnish)
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allele frequency: 1.522842639593909e-3
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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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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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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African
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Latino
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Other
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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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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GenotypeDepth
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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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European (Non-Finnish)
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South Asian
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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FS
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East Asian
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South Asian
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European (Finnish)
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African
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MQRankSum
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BaseQRankSum
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DP
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FS
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MQ
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VQSLOD
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all individuals: 1728
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26286
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.65508109897385e-4
allele num: 6042
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 9.92964e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

GenotypeDepth
all individuals: 670
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15187
bin: 7.5e0
variant carriers: 0

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

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

GenotypeDepth
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1115
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16387
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27233
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.75e1
variant carriers: 3